FAMOTIDINE
NDC 70377-113, FAMOTIDINE, powder, for suspension, from Biocon Pharma Inc..
- Product NDC
- 70377-113
- Status
- Listed
- Labeler
- Biocon Pharma Inc.
- 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/70377-113 \ -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 |
|---|---|---|
| 70377-113-11 | 70377011311 | 50 mL in 1 BOTTLE (70377-113-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/ea7287a4-75e0-39d2-5b2e-b72b7cb386b9NADAC price for package 70377011311
GET /v1/drugs/nadac/70377011311
Use it
Look up 70377-113 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70377-113 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70377-113. 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.