PRAVASTATIN SODIUM
NDC 71610-884, PRAVASTATIN SODIUM, tablet, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-884
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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/71610-884 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PRAVASTATIN SODIUM40 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71610-884-45 | 71610088445 | 45 TABLET in 1 BOTTLE (71610-884-45) |
| 71610-884-53 | 71610088453 | 60 TABLET in 1 BOTTLE (71610-884-53) |
| 71610-884-60 | 71610088460 | 90 TABLET in 1 BOTTLE (71610-884-60) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/308db0cc-0deb-99b6-e063-6394a90a9b74
Use it
Look up 71610-884 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-884 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-884. 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.