Simvastatin
- Product NDC
- 0179-1899
- 11-digit product format
- 001791899
- Labeler code
- 0179
- Product ID
- 0179-1899_7c4e5a6a-da5a-5992-e053-2a91aa0a71b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA076052
- Marketing category
- ANDA
- Marketing start
- 2016-09-28
- Marketing end
- 2019-05-31
- Substance
- SIMVASTATIN
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record