FAMOTIDINE
NDC 80005-119, FAMOTIDINE, powder, for suspension, from Carnegie Pharmaceuticals LLC.
- Product NDC
- 80005-119
- Status
- Listed
- Labeler
- Carnegie Pharmaceuticals LLC
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217137
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/80005-119 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FAMOTIDINE40 mg/5mL
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 80005-119-16 | 80005011916 | 50 mL in 1 BOTTLE (80005-119-16) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/45df5fae-b28a-4b48-95ef-96e4faad883fNADAC price for package 80005011916
GET /v1/drugs/nadac/80005011916
Use it
Look up 80005-119 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80005-119 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80005-119. 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.