FDA National Drug Codes
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FDA National Drug Codes
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FDA National Drug Codes
Browse every product in the FDA NDC Directory below, or search by NDC, brand, generic, manufacturer or HCPCS code. Each product has its own page with package NDCs in 11-digit billing format.
11,723 products (finished products)
| Product | Strength | Form · route | Labeler | Application | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|---|---|
| Aleve Back and Muscle Painnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-6092 | 00280-6092-0200280-6092-0400280-6092-05+6 more | — |
| Aleve Capletsnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-0114 | 00280-0114-0100280-0114-0200280-0114-03+3 more | — |
| Aleve Capletsnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-6000 | 00280-6000-0100280-6000-0200280-6000-03 |
| — |
| Aleve Capletsnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Select Consumer Group | NDA | 85237-1832 | 85237-1832-0185237-1832-0285237-1832-04+2 more | — |
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| Aleve Caplets - Easy Open Arthritis Capnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-6050 | 00280-6050-0100280-6050-0200280-6050-03+5 more | — |
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| Aleve Caplets Easy Open Arthritisnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-0130 | 00280-0130-0100280-0130-02 | — |
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| Aleve Caplets Soft Grip Arthritisnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-0115 | 00280-0115-0100280-0115-0200280-0115-03 | — |
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| Aleve Easy Open Arthritisnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-0131 | 00280-0131-01 | — |
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| Aleve Easy Open Arthritis Capnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-6060 | 00280-6060-2000280-6060-2500280-6060-32 | — |
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| Aleve Easy Open Arthritis Capnaproxen sodium | Naproxen sodium 220 mg/1 | Capsule, Liquid filledOral | Bayer HealthCare LLC. | NDA | 0280-6091 | 00280-6091-80 | — |
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| Aleve Gelcapsnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Bayer HealthCare LLC. | NDA | 0280-6020 | 00280-6020-0200280-6020-16 | — |
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| Aleve Gelcapsnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Bayer HealthCare LLC. | NDA | 0280-6070 | 00280-6070-40 | — |
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| Aleve Headache Painnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC | NDA | 0280-0041 | 00280-0041-0100280-0041-0200280-0041-03+2 more | — |
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| Aleve Headache Painnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-0112 | 00280-0112-0100280-0112-0200280-0112-03+1 more | — |
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| Aleve Headache Painnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | NDA | 0280-8252 | 00280-8252-1000280-8252-24 | — |
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| Aleve liquid gelsnaproxen sodium | Naproxen sodium 220 mg/1 | Capsule, Liquid filledOral | Bayer Healthcare LLC | ANDA | 0280-0105 | 00280-0105-0100280-0105-0200280-0105-03+3 more | — |
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| Aleve PMdiphenhydramine hydrochloride and naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Bayer HealthCare LLC. | NDA | 0280-1200 | 00280-1200-0100280-1200-0200280-1200-03+6 more | — |
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| Aleve, TRAVEL BASIXnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Lil' Drug Store Products, Inc | NDA | 66715-6411 | 66715-6411-02 | — |
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| Aleve-D Sinus and Coldnaproxen sodium, pseudeoephedrine hydrochloride | Pseudoephedrine hydrochloride 120 mg/1; Naproxen sodium 220 mg/1 | TabletOral | Bayer HealthCare LLC. | ANDA | 0280-6090 | 00280-6090-1000280-6090-20 | — |
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| Aleve-D Sinus and Headachenaproxen sodium, pseudoephedrine hydrochloride | Naproxen sodium 220 mg/1; Pseudoephedrine hydrochloride 120 mg/1 | TabletOral | Bayer HealthCare LLC. | ANDA | 0280-6045 | 00280-6045-10 | — |
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| AleveXcamphor and menthol | Camphor (Synthetic) 5.5 mg/g; Menthol 16 mg/g | SprayTopical | Bayer HealthCare LLC | OTC monograph drug | 0280-0049 | 00280-0049-01 | — |
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| AleveXcamphor and menthol | Menthol 16 mg/g; Camphor (Synthetic) 5.5 mg/g | LotionTopical | Bayer HealthCare LLC | OTC monograph drug | 0280-0050 | 00280-0050-01 | — |
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| AleveXcamphor and menthol | Camphor (Synthetic) 5.5 mg/g; Menthol 16 mg/g | LotionTopical | Bayer HealthCare LLC | OTC monograph drug | 0280-0063 | 00280-0063-01 | — |
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| ALEX MD PHD Sheer Mineral Sunscreenzinc oxide, titanium dioxide | Zinc oxide 20.2 g/100g; Titanium dioxide 6.8 g/100g | CreamTopical | PHYSICIAN LABORATORIES INC | OTC monograph drug | 78709-001 | 78709-0001-01 | — |
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| ALEX MD PHD Tinted Mineral Sunscreenzinc oxide, titanium dioxide | Zinc oxide 20.2 g/100g; Titanium dioxide 6.8 g/100g | CreamTopical | PHYSICIAN LABORATORIES INC | OTC monograph drug | 78709-002 | 78709-0002-01 | — |
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| Alfalfa | Alfalfa 6 [hp_C]/6[hp_C] | PelletOral | Boiron | Unapproved homeopathic | 0220-0161 | 00220-0161-41 | — |
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| Alfalfa | Alfalfa 6 [hp_X]/6[hp_X] | PelletOral | Boiron | Unapproved homeopathic | 0220-0164 | 00220-0164-41 | — |
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| Alfalfamedicago sativa | Medicago sativa pollen .02 g/mL | SolutionIntradermal, Percutaneous, Subcutaneous | Greer Laboratories, Inc. | BLA | 22840-1507 | 22840-1507-0222840-1507-04 | — |
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| Alfalfamedicago sativa | Medicago sativa pollen 1000 [PNU]/mL | SolutionIntradermal, Percutaneous, Subcutaneous | Greer Laboratories, Inc. | BLA | 22840-1508 | 22840-1508-01 | — |
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| Alfalfamedicago sativa | Medicago sativa pollen .001 g/mL | SolutionIntradermal, Percutaneous, Subcutaneous | Greer Laboratories, Inc. | BLA | 22840-1509 | 22840-1509-01 | — |
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| Alfalfamedicago sativa | Medicago sativa pollen 10000 [PNU]/mL | SolutionIntradermal, Percutaneous, Subcutaneous | Greer Laboratories, Inc. | BLA | 22840-1561 | 22840-1561-0222840-1561-04 | — |
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| Alfalfamedicago sativa | Medicago sativa pollen .02 g/mL | SolutionIntradermal, Percutaneous, Subcutaneous | Greer Laboratories, Inc. | BLA | 22840-5503 | 22840-5503-0222840-5503-0322840-5503-04+1 more | — |
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| Alfalfa Pollenmedicago sativa | Medicago sativa pollen .02 g/mL | InjectionCutaneous, Intradermal, Subcutaneous | Allermed Laboratories, Inc. | BLA | 49643-300 | 49643-0300-0549643-0300-1049643-0300-30+1 more | — |
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| Alfuzosin hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Unichem Pharmaceuticals (USA), Inc. | ANDA | 29300-155 | 29300-0155-0129300-0155-1329300-0155-19 | — |
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| Alfuzosin hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Aphena Pharma Solutions - Tennessee, LLC | ANDA | 43353-945 | 43353-0945-1643353-0945-3043353-0945-60 | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Sun Pharmaceutical Industries, Inc. | ANDA | 47335-956 | 47335-0956-0847335-0956-1847335-0956-81+2 more | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Film coated, Extended releaseOral | Northwind Health Company, LLC | ANDA | 51655-087 | 51655-0087-52 | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Northwind Health Company, LLC | ANDA | 51655-432 | 51655-0432-52 | — |
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| Alfuzosin hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Northwind Health Company, LLC | ANDA | 51655-967 | 51655-0967-52 | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Film coated, Extended releaseOral | Rising Pharma Holdings, Inc. | ANDA | 57237-114 | 57237-0114-0157237-0114-0557237-0114-90 | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Apotex Corp. | ANDA | 60505-2850 | 60505-2850-09 | — |
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| Alfuzosin hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | ANDA | 63629-9155 | 63629-9155-0163629-9155-0263629-9155-03+1 more | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Film coated, Extended releaseOral | Aurobindo Pharma Limited | ANDA | 65862-249 | 65862-0249-0165862-0249-0565862-0249-30+2 more | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | ANDA | 71335-2146 | 71335-2146-0171335-2146-0271335-2146-03+2 more | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Film coated, Extended releaseOral | Bryant Ranch Prepack | ANDA | 71335-2578 | 71335-2578-0171335-2578-0271335-2578-03+2 more | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Bryant Ranch Prepack | ANDA | 72162-1449 | 72162-1449-09 | — |
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| Alfuzosin hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Extended releaseOral | Exelan Pharmaceuticals Inc. | ANDA | 76282-302 | 76282-0302-0176282-0302-0576282-0302-10+2 more | — |
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| Alfuzosin Hydrochloride | Alfuzosin hydrochloride 10 mg/1 | Tablet, Film coated, Extended releaseOral | Aurobindo Pharma Limited | ANDA | 84386-153 | 84386-0153-0184386-0153-0584386-0153-30+2 more | — |
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| Alfuzosin Hydrochloride extended releasealfuzosin hydrochloride | Alfuzosin hydrochloride 10 mg/1 | TabletOral | Cipla USA Inc. | ANDA | 69097-844 | 69097-0844-0269097-0844-0569097-0844-07+1 more | — |
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| Algenistoctinoxate, titanium dioxide, zinc oxide | Octinoxate 75 mg/mL + 2 more ingredients | CreamTopical | Solazyme, Inc. | OTC monograph drug | 53407-138 | 53407-0138-30 | — |
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