Pravastatin Sodium
- Product NDC
- 70518-0423
- 11-digit product format
- 705180423
- Labeler code
- 70518
- Product ID
- 70518-0423_84ff5a1c-9f60-a03c-e053-2991aa0a3481
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077987
- Marketing category
- ANDA
- Marketing start
- 2017-04-12
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 20 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