Famotidine
NDC 71335-2190, Famotidine, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-2190
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216441
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2190 \ -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 |
|---|---|---|
| 71335-2190-1 | 71335219001 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2190-1) |
| 71335-2190-2 | 71335219002 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2190-2) |
| 71335-2190-3 | 71335219003 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2190-3) |
| 71335-2190-4 | 71335219004 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2190-4) |
| 71335-2190-5 | 71335219005 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2190-5) |
| 71335-2190-6 | 71335219006 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2190-6) |
| 71335-2190-7 | 71335219007 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2190-7) |
| 71335-2190-8 | 71335219008 | 50 TABLET, FILM COATED in 1 BOTTLE (71335-2190-8) |
| 71335-2190-9 | 71335219009 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-2190-9) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/72a97532-9a79-4cbf-b9d0-22ce1f21468d
Use it
Look up 71335-2190 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2190 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2190. 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.