PRAVASTATIN SODIUM
- Product NDC
- 68788-7013
- 11-digit product format
- 687887013
- Labeler code
- 68788
- Product ID
- 68788-7013_c0a79a76-a9ce-4336-bf2d-9f41dbe68c9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2017-08-29
- 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