ATORVASTATIN CALCIUM
- Product NDC
- 63629-4796
- 11-digit product format
- 636294796
- Labeler code
- 63629
- Product ID
- 63629-4796_61d1133b-6839-4ef1-8de2-5b861a566e9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090548
- Marketing category
- ANDA
- Marketing start
- 2012-05-29
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-4796-1 | 63629479601 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4796-1) | 2012-11-29 | 0000-00-00 | No | No | Current |
| 63629-4796-2 | 63629479602 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4796-2) | 2012-12-13 | 0000-00-00 | No | No | Current |
| 63629-4796-3 | 63629479603 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4796-3) | 2019-06-28 | 0000-00-00 | No | No | Current |
| 63629-4796-4 | 63629479604 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-4796-4) | 2015-03-16 | 0000-00-00 | No | No | Current |
| 63629-4796-5 | 63629479605 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-4796-5) | 2019-09-04 | 0000-00-00 | No | No | Current |
| 63629-4796-6 | 63629479606 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-4796-6) | 2021-12-22 | 0000-00-00 | No | No | Current |