Atorvastatin Calcium
- Product NDC
- 43353-182
- 11-digit product format
- 433530182
- Labeler code
- 43353
- Product ID
- 43353-182_751b826c-7e98-4ffc-8dd0-d4bb32d6fded
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA091226
- Marketing category
- ANDA
- Marketing start
- 2013-09-19
- Marketing end
- 2021-02-28
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 43353-182-45 | 43353018245 | 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-182-45) | 2016-06-02 | 2021-02-28 | No | No | Current |