Atorvastatin Calcium
- Product NDC
- 51655-614
- 11-digit product format
- 516550614
- Labeler code
- 51655
- Product ID
- 51655-614_30f9e52a-9799-4d3a-9392-d692c53d6047
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA091624
- Marketing category
- ANDA
- Marketing start
- 2015-08-25
- 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
FDA-Initiated Inactive NDC Indexing#