Famotidine
NDC 69367-401, Famotidine, tablet, coated, from Westminster Pharmaceuticals, LLC.
- Product NDC
- 69367-401
- Status
- Listed
- Labeler
- Westminster Pharmaceuticals, LLC
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217669
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69367-401 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FAMOTIDINE40 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69367-401-10 | 69367040110 | 1000 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-401-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c0e15f57-ab20-4030-b1d1-6aff33be7d76NADAC price for package 69367040110
GET /v1/drugs/nadac/69367040110
Use it
Look up 69367-401 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69367-401 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69367-401. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.