PRAVASTATIN SODIUM
- Product NDC
- 70518-1862
- 11-digit product format
- 705181862
- Labeler code
- 70518
- Product ID
- 70518-1862_81b7c8e7-fc97-05d6-e053-2991aa0a473d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077917
- Marketing category
- ANDA
- Marketing start
- 2019-02-12
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record