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.
4,454 products (finished products)
| Product | Strength | Form · route | Labeler | Application | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|---|---|
| Enoxaparin Sodium | Enoxaparin sodium 150 mg/mL | InjectionSubcutaneous | Meitheal Pharmaceuticals Inc. | ANDA | 71288-438 | 71288-0438-96 | — |
| enoxaparin sodium | Enoxaparin sodium 30 mg/.3mL | InjectionSubcutaneous | BE Pharmaceuticals Inc. | ANDA | 71839-109 | 71839-0109-10 | — |
| enoxaparin sodium | Enoxaparin sodium 40 mg/.4mL | InjectionSubcutaneous | BE Pharmaceuticals Inc. | ANDA | 71839-110 | 71839-0110-10 | — |
| enoxaparin sodium | Enoxaparin sodium 60 mg/.6mL | InjectionSubcutaneous | BE Pharmaceuticals Inc. | ANDA |
| 71839-111 |
| 71839-0111-10 |
| — |
| enoxaparin sodium | Enoxaparin sodium 80 mg/.8mL | InjectionSubcutaneous | BE Pharmaceuticals Inc. | ANDA | 71839-112 | 71839-0112-10 | — |
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| enoxaparin sodium | Enoxaparin sodium 100 mg/mL | InjectionSubcutaneous | BE Pharmaceuticals Inc. | ANDA | 71839-113 | 71839-0113-10 | — |
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| enoxaparin sodium | Enoxaparin sodium 120 mg/.8mL | InjectionSubcutaneous | BE Pharmaceuticals Inc. | ANDA | 71839-115 | 71839-0115-10 | — |
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| enoxaparin sodium | Enoxaparin sodium 150 mg/mL | InjectionSubcutaneous | BE Pharmaceuticals Inc. | ANDA | 71839-116 | 71839-0116-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 100 mg/mL | InjectionSubcutaneous | Civica, Inc. | ANDA | 72572-280 | 72572-0280-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 30 mg/.3mL | Injection, SolutionSubcutaneous | NorthStar RxLLC | ANDA | 72603-165 | 72603-0165-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 40 mg/.4mL | Injection, SolutionSubcutaneous | NorthStar RxLLC | ANDA | 72603-175 | 72603-0175-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 60 mg/.6mL | Injection, SolutionSubcutaneous | NorthStar RxLLC | ANDA | 72603-185 | 72603-0185-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 80 mg/.8mL | Injection, SolutionSubcutaneous | NorthStar RxLLC | ANDA | 72603-195 | 72603-0195-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 100 mg/mL | Injection, SolutionSubcutaneous | NorthStar RxLLC | ANDA | 72603-205 | 72603-0205-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 120 mg/.8mL | Injection, SolutionSubcutaneous | NorthStar RxLLC | ANDA | 72603-215 | 72603-0215-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 150 mg/mL | Injection, SolutionSubcutaneous | NorthStar RxLLC | ANDA | 72603-225 | 72603-0225-10 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 30 mg/.3mL | Injection, SolutionSubcutaneous | Hepalink USA Inc. | ANDA | 81952-123 | 81952-0123-23 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 40 mg/.4mL | Injection, SolutionSubcutaneous | Hepalink USA Inc. | ANDA | 81952-124 | 81952-0124-24 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 60 mg/.6mL | Injection, SolutionSubcutaneous | Hepalink USA Inc. | ANDA | 81952-126 | 81952-0126-26 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 80 mg/.8mL | Injection, SolutionSubcutaneous | Hepalink USA Inc. | ANDA | 81952-128 | 81952-0128-28 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 100 mg/mL | Injection, SolutionSubcutaneous | Hepalink USA Inc. | ANDA | 81952-130 | 81952-0130-06 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 120 mg/.8mL | Injection, SolutionSubcutaneous | Hepalink USA Inc. | ANDA | 81952-132 | 81952-0132-28 | — |
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| Enoxaparin Sodium | Enoxaparin sodium 150 mg/mL | Injection, SolutionSubcutaneous | Hepalink USA Inc. | ANDA | 81952-135 | 81952-0135-06 | — |
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| Enoxiluv Kitenoxaparin sodium, isopropyl alcohol | — | KitSubcutaneous, Topical | Asclemed USA, Inc. | Unapproved drug (other) | 76420-532 | 76420-0532-01 | — |
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| Enriched Foam Alcohol-Free Hand Sanitizerbenzalkonium chloride | Benzalkonium chloride 13 mg/100mL | LiquidTopical | Rubbermaid Commercial Products LLC | OTC monograph drug | 65321-039 | 65321-0039-01 | — |
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| Ensacoveensartinib | Ensartinib hydrochloride 25 mg/1 | CapsuleOral | Xcovery Holdings, Inc. | NDA | 83076-1025 | 83076-1025-03 | — |
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| Ensacoveensartinib | Ensartinib hydrochloride 100 mg/1 | CapsuleOral | Xcovery Holdings, Inc. | NDA | 83076-1100 | 83076-1100-06 | — |
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| Enskycedesogestrel and ethinyl estradiol | — | Kit | Lupin Pharmaceuticals, Inc. | ANDA | 68180-739 | 68180-0739-73 | — |
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| Enspryngsatralizumab | Satralizumab 120 mg/mL | Injection, SolutionSubcutaneous | Genentech, Inc. | BLA | 50242-007 | 50242-0007-0150242-0007-3350242-0007-55+1 more | — |
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| Enstilarcalcipotriene and betamethasone dipropionate | Calcipotriene monohydrate 50 ug/g; Betamethasone dipropionate .5 mg/g | Aerosol, FoamTopical | LEO Pharma Inc. | NDA | 50222-302 | 50222-0302-6050222-0302-6650222-0302-91 | — |
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| ENT Essentials All Dry Ear Drying Dropsisopropyl alcohol | Isopropyl alcohol .95 g/100g | LiquidAuricular (Otic) | Wisconsin Pharmacal Company | OTC monograph (final) | 68093-4501 | 68093-4501-01 | — |
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| ENT Essentials Ear Wax Remvoercarbamide peroxide | Carbamide peroxide .065 g/g | LiquidAuricular (Otic) | Wisconsin Pharmacal Company | OTC monograph (not final) | 68093-4503 | 68093-4503-01 | — |
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| ENT Supportpulsatilla (pratensis), euphorbium officinarum, luffa operculata, mercurius iodatus ruber, argentum nitricum, hepar sulphuris calcareum, influenzinum (2021-2022), sinusitisinum, aspergillus niger, candida albicans, gallicum acidum, mucor racemosus, mutabile bacillus (bach) | Pulsatilla pratensis whole 4 [hp_X]/mL + 15 more ingredients | LiquidOral | Deseret Biologicals, Inc. | Unapproved homeopathic | 43742-2041 | 43742-2041-01 | — |
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| ENT Supportpulsatilla (pratensis), euphorbium officinarum, luffa operculata, mercurius iodatus ruber, argentum nitricum, hepar sulphuris calcareum, influenzinum (2022-2023), sinusitisinum, aspergillus niger, candida albicans, gallicum acidum, mucor racemosus, mutabile bacillus (bach) | Pulsatilla pratensis whole 4 [hp_X]/mL + 15 more ingredients | LiquidOral | Deseret Biologicals, Inc. | Unapproved homeopathic | 43742-2061 | 43742-2061-01 | — |
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| ENT Supportargentum nitricum, aspergillus niger, candida albicans, euphorbium officinarum, gallicum acidum, hepar sulphuris calcareum, influenzinum (2023-2024), luffa operculata, mercurius iodatus ruber, mucor racemosus, mutabile bacillus (bach), pulsatilla (pratensis), sinusitisinum | Silver nitrate 10 [hp_X]/mL + 15 more ingredients | LiquidOral | Deseret Biologicals, Inc. | Unapproved homeopathic | 43742-2142 | 43742-2142-01 | — |
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| ENT Supportargentum nitricum, aspergillus niger, candida albicans, euphorbium officinarum, gallicum acidum, hepar sulphuris calcareum, influenzinum (2024 - 2025), luffa operculata, mercurius iodatus ruber, mucor racemosus, mutabile bacillus (bach), pulsatilla (pratensis), sinusitisinum | Silver nitrate 10 [hp_X]/mL + 15 more ingredients | LiquidOral | Deseret Biologicals, Inc. | Unapproved homeopathic | 43742-2358 | 43742-2358-01 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Lannett Company, Inc. | ANDA | 0527-1830 | 00527-1830-37 | — |
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| Entacapone | Entacapone 200 mg/1 | TabletOral | NCS HealthCare of KY, LLC dba Vangard Labs | ANDA | 0615-8298 | 00615-8298-39 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Sandoz Inc | NDA authorized generic | 0781-5578 | 00781-5578-01 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Major Pharmaceuticals | ANDA | 0904-6822 | 00904-6822-07 | — |
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| Entacapone | Entacapone 200 mg/1 | TabletOral | Ajanta Pharma USA Inc. | ANDA | 27241-049 | 27241-0049-10 | — |
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| Entacapone | Entacapone 200 mg/1 | TabletOral | Macleods Pharmaceuticals Limited | ANDA | 33342-260 | 33342-0260-1133342-0260-15 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Alembic Pharmaceuticals Limited | ANDA | 46708-478 | 46708-0478-3146708-0478-91 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | NDA authorized generic | 47335-007 | 47335-0007-88 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | AvPAK | ANDA | 50268-295 | 50268-0295-15 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | American Health Packaging | ANDA | 60687-188 | 60687-0188-21 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Alembic Pharmaceuticals Inc. | ANDA | 62332-478 | 62332-0478-3162332-0478-91 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Rising Pharma Holdings, Inc. | ANDA | 64980-722 | 64980-0722-01 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | ANDA | 65862-654 | 65862-0654-0165862-0654-99 | — |
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| Entacapone | Entacapone 200 mg/1 | Tablet, Film coatedOral | Aphena Pharma Solutions - Tennessee, LLC | NDA authorized generic | 71610-247 | 71610-0247-83 | — |
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