Atorvastatin Calcium
- Product NDC
- 68788-6331
- 11-digit product format
- 687886331
- Labeler code
- 68788
- Product ID
- 68788-6331_1d040029-96a7-4fbf-8cc0-7087aaabd395
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091650
- Marketing category
- ANDA
- Marketing start
- 2012-07-17
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record