simvastatin
- Product NDC
- 0179-0241
- 11-digit product format
- 001790241
- Labeler code
- 0179
- Product ID
- 0179-0241_7b0d2dce-d057-1f38-e053-2a91aa0a22ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA078155
- Marketing category
- ANDA
- Marketing start
- 2018-04-05
- Marketing end
- 2020-01-31
- Substance
- SIMVASTATIN
- Active strength
- 20 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