PRAVASTATIN SODIUM
- Product NDC
- 70518-1710
- 11-digit product format
- 705181710
- Labeler code
- 70518
- Product ID
- 70518-1710_962f18e7-922f-a44d-e053-2a95a90abafe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2018-12-05
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 80 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