Simvastatin
- Product NDC
- 51079-456
- 11-digit product format
- 510790456
- Labeler code
- 51079
- Product ID
- 51079-456_9af1b4b7-abf7-2bc7-e053-2a95a90a6153
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA076052
- Marketing category
- ANDA
- Marketing start
- 2006-07-10
- Marketing end
- 2020-05-31
- Substance
- SIMVASTATIN
- Active strength
- 40 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