NDC SPL data elements
Every package NDC listed in drug labeling, with its marketing category, dates and application number. 672,578 records; openFDA updated it 2026-11-13. About this dataset
Newest records
- ANDA262,693
- OTC Monograph Drug100,764
- OTC monograph not final83,531
- unapproved homeopathic52,802
- NDA45,540
- OTC monograph final27,921
- unapproved drug other25,815
- BLA25,038
- Sun Bum Spf 30 Lip Balm Tube Banana Cream
OINTMENT · HUMAN OTC DRUG · M020
- Sucralfate
TABLET · HUMAN PRESCRIPTION DRUG · ANDA215705
- Fungi Nail Toe And Foot
OINTMENT · HUMAN OTC DRUG · M005
- Glowscreen Spf 50 - Golden Hour
LOTION · HUMAN OTC DRUG · M020
- Glowscreen Spf 50 - Daybreak
LOTION · HUMAN OTC DRUG · M020
- Dove
STICK · HUMAN OTC DRUG · M019
- Glowscreen Spf 50 - Sunrise
LOTION · HUMAN OTC DRUG · M020
- Glowscreen Spf 50 - Sunrise
LOTION · HUMAN OTC DRUG · M020
- Yesafili
INJECTION, SOLUTION · HUMAN PRESCRIPTION DRUG · BLA761274
- Glowscreen Spf 50 - Sunrise
LOTION · HUMAN OTC DRUG · M020
- Eagle Brand Massage Balm
OINTMENT · HUMAN OTC DRUG · M017
- Utebzi
TABLET, FILM COATED · HUMAN PRESCRIPTION DRUG · NDA215960
- Cyclophosphamide
CAPSULE · HUMAN PRESCRIPTION DRUG · ANDA210890
- Sucralfate
TABLET · HUMAN PRESCRIPTION DRUG · ANDA215705
- Dove
STICK · HUMAN OTC DRUG · M019
- Potassium Chloride Extended-Release
TABLET, EXTENDED RELEASE · HUMAN PRESCRIPTION DRUG · ANDA209688
- Tramadol Hydrochloride
TABLET · HUMAN PRESCRIPTION DRUG · ANDA075968
- Kacsur 5% Minoxidil With Biotin Topical Solution
AEROSOL, FOAM · HUMAN OTC DRUG · M032
- Glowscreen Spf 50 - Sunrise
LOTION · HUMAN OTC DRUG · M020
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.
