Atorvastatin Calcium
- Product NDC
- 35356-860
- 11-digit product format
- 353560860
- Labeler code
- 35356
- Product ID
- 35356-860_c6b13215-f342-4c0e-99a3-18a43d1aba0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA091650
- Marketing category
- ANDA
- Marketing start
- 2012-07-17
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM
- 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