Simvastatin
- Product NDC
- 55154-9525
- 11-digit product format
- 551549525
- Labeler code
- 55154
- Product ID
- 55154-9525_3f0f17e1-a96b-4f45-8dcf-95a2065c532e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA078034
- Marketing category
- ANDA
- Marketing start
- 2011-10-17
- Marketing end
- 0000-00-00
- Substance
- SIMVASTATIN
- Active strength
- 5 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record