Famotidine
NDC 0641-6021, Famotidine, injection, from Hikma Pharmaceuticals USA Inc..
- Product NDC
- 0641-6021
- Status
- Listed
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075488
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6021 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FAMOTIDINE10 mg/mL
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0641-6021-10 | 00641602110 | 10 VIAL in 1 CARTON (0641-6021-10) / 20 mL in 1 VIAL (0641-6021-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1fdf16e5-145d-4c19-a318-fc6c10794b50Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=0641-6021
Use it
Look up 0641-6021 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6021 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0641-6021. 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.