FAMOTIDINE
NDC 67877-889, FAMOTIDINE, tablet, film coated, from Ascend Laboratories, LLC.
- Product NDC
- 67877-889
- Status
- Listed
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215630
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/67877-889 \ -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 |
|---|---|---|
| 67877-889-01 | 67877088901 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-889-01) |
| 67877-889-05 | 67877088905 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-889-05) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/be69d9f9-f4ad-4cfe-bab2-e07186b25c1eNADAC price for package 67877088901
GET /v1/drugs/nadac/67877088901NADAC price for package 67877088905
GET /v1/drugs/nadac/67877088905
Use it
Look up 67877-889 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/67877-889 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 67877-889. 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.