Atorvastatin Calcium
- Product NDC
- 50090-1258
- 11-digit product format
- 500901258
- Labeler code
- 50090
- Product ID
- 50090-1258_31c01d4c-6259-40c9-b201-612eeb69805a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091624
- Marketing category
- ANDA
- Marketing start
- 2013-04-05
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1258-0 | 50090125800 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1258-0) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1258-1 | 50090125801 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1258-1) | 2014-11-28 | 0000-00-00 | No | No | Current |