Famotidine
NDC 71335-2805, Famotidine, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-2805
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217400
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2805 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FAMOTIDINE20 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-2805-0 | 71335280500 | 40 TABLET, FILM COATED in 1 BOTTLE (71335-2805-0) |
| 71335-2805-1 | 71335280501 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2805-1) |
| 71335-2805-2 | 71335280502 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2805-2) |
| 71335-2805-3 | 71335280503 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2805-3) |
| 71335-2805-4 | 71335280504 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2805-4) |
| 71335-2805-5 | 71335280505 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2805-5) |
| 71335-2805-6 | 71335280506 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2805-6) |
| 71335-2805-7 | 71335280507 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2805-7) |
| 71335-2805-8 | 71335280508 | 50 TABLET, FILM COATED in 1 BOTTLE (71335-2805-8) |
| 71335-2805-9 | 71335280509 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-2805-9) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c133a9e1-ca48-4ee2-8768-01f44f5dd511
Use it
Look up 71335-2805 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2805 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2805. 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.