FAMOTIDINE
NDC 31722-063, FAMOTIDINE, powder, for suspension, from Camber Pharmaceuticals, Inc..
- Product NDC
- 31722-063
- Status
- Listed
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217330
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/31722-063 \ -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 |
|---|---|---|
| 31722-063-31 | 31722006331 | 50 mL in 1 BOTTLE (31722-063-31) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/8e7f9c85-d165-47c7-8950-b22adcd6ceceNADAC price for package 31722006331
GET /v1/drugs/nadac/31722006331
Use it
Look up 31722-063 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/31722-063 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 31722-063. 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.