Pravastatin sodium
- Product NDC
- 68788-7193
- 11-digit product format
- 687887193
- Labeler code
- 68788
- Product ID
- 68788-7193_77d581ee-7d09-4408-ab06-336c3a8e482e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076714
- Marketing category
- ANDA
- Marketing start
- 2018-07-18
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record