ATORVASTATIN CALCIUM
- Product NDC
- 60760-354
- 11-digit product format
- 607600354
- Labeler code
- 60760
- Product ID
- 60760-354_8ccbb03e-fb2d-8665-e053-2995a90a356e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- ANDA090548
- Marketing category
- ANDA
- Marketing start
- 2014-04-20
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record