Every drug product currently marketed in the US — prescription, OTC, homeopathic, vaccine, plasma derivative, cellular therapy, allergenic. **134,944 unique product NDCs**. Each NDC carries: brand + generic name, labeler (legal seller), manufacturer name(s), dosage form (TABLET / CAPSULE / INJECTION / etc), administration route (ORAL / INTRAMUSCULAR / TOPICAL / etc), pharmacological class (e.g. "HMG-CoA Reductase Inhibitor"), marketing category (NDA innovator / ANDA generic / BLA biologic / OTC monograph / Unapproved drug), FDA application number (joins to drug_approvals), UNII codes for active substances, SPL Set ID (joins to DailyMed labels), marketing start + end dates, package count, active ingredients with strengths. Source: openFDA `drug/ndc.json` (no auth, weekly refresh, CC0). Foundational drug-product layer that joins NDA approvals + RxNorm + DailyMed labels + adverse events + warning letters.
This dataset was ingested from the listed source URL. Ingestion source: https://open.fda.gov/apis/drug/ndc/. Source-specific terms apply. US federal employee-authored works are generally public domain under 17 USC 105; non-federal and third-party material retains source terms. Free or keyless access does not alter source terms. Metadata and normalization authored by MORVS (AI Analytics LLC) are CC0 only where expressly stated.