FDA NDC Directory
NDC Codes — National Drug Codes
Look up any National Drug Code, or browse the FDA NDC Directory by drug, active ingredient or labeler. Every product has its own page with package NDCs in 10- and 11-digit form.
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Drugs by name
Active ingredients
Labelers
NDC directory: A
The first products in brand-name order. Browse every NDC, 50 to a page, A to Z.
| Product | Strength | Form · route | Labeler | Application | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|---|---|
| A and Dpetrolatum | Petrolatum 76 g/100g | OintmentTopical | Safetec of America, Inc. | OTC monograph drug | 61010-4405 | 61010-4405-01 | — |
| A and D Diaper Rash and Skin Protectantlanolin and petrolatum | Lanolin .15 mg/g; Petrolatum .53 mg/g | CreamTopical | Natureplex LLC | OTC monograph drug | 67234-030 | 67234-0030-01 | — |
| A and D plus Evitamin a, d and e ointment | Petrolatum .9985 g/g | OintmentTopical | Derma Sciences Canada Inc. | OTC monograph drug | 64772-200 | 64772-0200-0364772-0200-0464772-0200-05 | — |
| A and E Deep Throat Desensitizing SprayPeppermintoral numbing spray mint | Benzocaine 3 mg/100mL | SprayTopical | Phe Inc | OTC monograph drug | 87068-182 | 87068-0182-11 | — |
| A and E Deep Throat Desensitizing SprayStrawberryoral numbing spray strawberry | Benzocaine 3 mg/100mL | SprayTopical | Phe Inc | OTC monograph drug | 87068-183 | 87068-0183-11 | — |
| A and E Easy Anal Gelanal numbing lubricant | Benzocaine 3.5 mg/100mL | SprayTopical | Phe Inc | OTC monograph drug | 87068-184 | 87068-0184-11 | — |
| A and E Marathon Delay Serumdelay serum | Benzocaine 7.5 mg/100mL | CreamTopical | Phe Inc | OTC monograph drug | 87068-181 | 87068-0181-11 | — |
| A and H Plus Therabreath Breath Freshnerssodium fluoride | Sodium fluoride .243 g/100g | Paste, DentifriceOral | Church & Dwight Co., Inc. | OTC monograph drug | 10237-676 | 10237-0676-0910237-0676-4510237-0676-51+2 more | — |
| A Health Itch Relief Gelitch relief gel | Diphenhydramine hydrochloride 2 mg/100mL | GelTopical | Bionpharma, Inc. | OTC monograph drug | 69452-376 | 69452-0376-55 | — |
| A Health Itch Relief Gelitch relief gel | Diphenhydramine hydrochloride 2 mg/100mL | GelTopical | Bionpharma, Inc. | OTC monograph drug | 69452-496 | 69452-0496-55 | — |
| A Health Itch Relief Gelitch relief gel | Diphenhydramine hydrochloride 2 mg/100mL | GelTopical | Pharma Nobis, LLC | OTC monograph drug | 82645-116 | 82645-0116-94 | — |
| A L O Formulacholinum, l-arginine, l-carnitine, l-ornithine, pantothenic acid | Choline hydroxide 6 [hp_X]/mL + 4 more ingredients | SprayOral | Nutritional Specialties, Inc. | Unapproved homeopathic | 83027-0084 | 83027-0084-01 | — |
| A Perfect World SPF 40 Age Defense Broad Spectrum Moisturizer With White Teaavobenzone, homosalate, octinoxate, octisalate, and octocrylene | Avobenzone 30 mg/mL + 4 more ingredients | CreamTopical | ORIGINS NATURAL RESOURCES INC. | OTC monograph drug | 59427-010 | 59427-0010-01 | — |
| A plus Attentionbaryta carbonica, calcarea phosphorica, silicea, gelsemium sempervirens, nux vomica, sinapis nigra | Barium carbonate 10 [hp_X]/1 + 5 more ingredients | Tablet, ChewableOral | NaturalCare | Unapproved homeopathic | 70163-0033 | 70163-0033-02 | — |
| A-1capra hircus skin, felis catus skin, bos taurus skin, canis lupus familiaris skin, equus caballus skin, capra hircus hair, and sheep wool | Capra hircus skin 30 [hp_X]/mL + 6 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0293 | 58264-0293-01 | — |
| A-10quercus rubra whole, quercus velutina whole, quercus alba wood, quercus kelloggii whole, quercus agrifolia whole, and quercus garryana whole | Quercus rubra whole 30 [hp_X]/mL + 5 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0302 | 58264-0302-01 | — |
| A-11egg white and egg yolk | Egg white 30 [hp_X]/mL; Egg yolk 30 [hp_X]/mL | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0303 | 58264-0303-01 | — |
| A-12juniperus ashei pollen, juniperus virginiana pollen, tamarix gallica pollen, cupressus arizonica pollen, taxodium distichum pollen, juniperus monosperma pollen, juniperus pinchotii pollen, juniperus scopulorum pollen, pinus taeda pollen, pinus strobus pollen, and pinus echinata pollen | Juniperus ashei pollen 30 [hp_X]/mL + 10 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0304 | 58264-0304-01 | — |
| A-13gallus gallus feather, anas platyrhynchos feather, and anser anser feather | Gallus gallus feather 30 [hp_X]/mL + 2 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0305 | 58264-0305-01 | — |
| A-14cod, unspecified, flounder, unspecified, halibut, unspecified, mackerel, unspecified, tuna, unspecified, and salmon, unspecified | Cod, Unspecified 30 [hp_X]/mL + 5 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0306 | 58264-0306-01 | — |
| A-15apple, apricot, banana, cherry, grape, peach, pineapple, pear, and strawberry | Apple 30 [hp_X]/mL + 8 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0307 | 58264-0307-01 | — |
| A-16barley, corn, oat, and wheat | Barley 30 [hp_X]/mL + 3 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0308 | 58264-0308-01 | — |
| A-17barley, corn, oat, white rice, rye, and wheat | Barley 30 [hp_X]/mL + 5 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0309 | 58264-0309-01 | — |
| A-18ceiba pentandra seed, powdered cellulose, and bombyx mori fiber | Ceiba pentandra seed 30 [hp_X]/mL + 2 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0310 | 58264-0310-01 | — |
| A-19solenopsis invicta, periplaneta americana, musca domestica, bombyx mori whole, and aedes taeniorhynchus | Solenopsis invicta 30 [hp_X]/mL + 4 more ingredients | SolutionSublingual | DNA Labs, Inc. | Unapproved homeopathic | 58264-0311 | 58264-0311-01 | — |
What is an NDC code?
A National Drug Code is the FDA’s product identifier for human drugs in the United States. Every drug marketed in the US is listed with the FDA under an NDC. The number identifies a product and its package; it is not an approval, and a listing does not mean a drug is covered or clinically appropriate. More on what an NDC is.
How NDC numbers are structured
An NDC has three segments, separated by hyphens in the FDA’s 10-digit form:
- Labeler code (4 or 5 digits), assigned by the FDA to the company on the label. See the labeler directory.
- Product code (3 or 4 digits), assigned by the labeler to one strength and dosage form.
- Package code (1 or 2 digits), assigned by the labeler to one package size.
The labeler and product segments together are the product NDC; all three are the package NDC. NDC format in detail.
10-digit vs 11-digit NDC
The FDA publishes NDCs as 10 digits in a 4-4-2, 5-3-2 or 5-4-1 shape. HIPAA claims use an 11-digit 5-4-2 form, made by adding a leading zero to the short segment. Each product page on Med-Code shows both. How to convert.
How to find an NDC number
The NDC is printed on the drug’s package and label. To look one up, search by drug name, ingredient or labeler above, or browse the drug and ingredient directories. How to find and verify an NDC.
NDC vs HCPCS and J-codes
An NDC identifies a product and package. A HCPCS J-code describes a drug and a dose unit for billing, whoever made it. One J-code usually covers many NDCs, and drugs dispensed by a pharmacy are billed by NDC with no J-code. NDC vs J-code · J-code list.
NDC codes in medical billing
On a professional or institutional claim, a drug line carries the HCPCS code and units, plus the 11-digit NDC with a unit qualifier and quantity. NDC billing and units of measure.