Atorvastatin Calcium
- Product NDC
- 68071-4279
- 11-digit product format
- 680714279
- Labeler code
- 68071
- Product ID
- 68071-4279_64cd83a5-2ac7-425d-e053-2991aa0af338
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA091624
- Marketing category
- ANDA
- Marketing start
- 2013-04-05
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM
- Active strength
- 80 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
FDA-Initiated Inactive NDC Indexing#