Fosinopril Sodium
NDC 71335-0187, Fosinopril, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-0187
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077222
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0187 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FOSINOPRIL SODIUM20 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-0187-1 | 71335018701 | 30 TABLET in 1 BOTTLE (71335-0187-1) |
| 71335-0187-2 | 71335018702 | 28 TABLET in 1 BOTTLE (71335-0187-2) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6562a532-b502-4515-88df-591d71293b56
Use it
Look up 71335-0187 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0187 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0187. 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.