acid reducer
NDC 69842-659, famotidine, tablet, film coated, from CVS Pharmacy.
- Product NDC
- 69842-659
- Status
- Listed
- Labeler
- CVS Pharmacy
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA077351
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69842-659 \ -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 |
|---|---|---|
| 69842-659-63 | 69842065963 | 1 BOTTLE in 1 CARTON (69842-659-63) / 25 TABLET, FILM COATED in 1 BOTTLE |
| 69842-659-71 | 69842065971 | 1 BOTTLE in 1 CARTON (69842-659-71) / 50 TABLET, FILM COATED in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 69842-659 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69842-659 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69842-659. 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.