Atorvastatin Calcium
- Product NDC
- 43353-181
- 11-digit product format
- 433530181
- Labeler code
- 43353
- Product ID
- 43353-181_751b826c-7e98-4ffc-8dd0-d4bb32d6fded
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA091226
- Marketing category
- ANDA
- Marketing start
- 2013-09-19
- Marketing end
- 2020-12-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record