pravastatin sodium
- Product NDC
- 55154-4982
- 11-digit product format
- 551544982
- Labeler code
- 55154
- Product ID
- 55154-4982_a93926b7-be06-4279-9e7a-a028fef44144
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077751
- Marketing category
- ANDA
- Marketing start
- 2013-05-24
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SOD
- Active strength
- 20 mg/1
- Pharmacologic classes
- HMG-CoA Reducta
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record