PRAVASTATIN SODIUM
NDC 72162-1951, PRAVASTATIN SODIUM, tablet, from Bryant Ranch Prepack.
- Product NDC
- 72162-1951
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209869
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1951 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PRAVASTATIN SODIUM10 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-1951-0 | 72162195100 | 1000 TABLET in 1 BOTTLE (72162-1951-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7b7f5c28-78fa-4625-ad69-4291500e033d
Use it
Look up 72162-1951 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1951 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-1951. 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.