ATORVASTATIN CALCIUM
- Product NDC
- 60760-353
- 11-digit product format
- 607600353
- Labeler code
- 60760
- Product ID
- 60760-353_7a01ce57-930d-7b1f-e053-2991aa0a0d75
- 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
- 10 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