Atorvastatin Calcium
- Product NDC
- 71335-1641
- 11-digit product format
- 713351641
- Labeler code
- 71335
- Product ID
- 71335-1641_2ef79cdf-2d3a-4424-b140-7ae11808c7ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076477
- Marketing category
- ANDA
- Marketing start
- 2011-12-01
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 71335-1641-1 | 71335164101 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1641-1) | 2022-02-28 | 0000-00-00 | No | No | Current |
| 71335-1641-2 | 71335164102 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1641-2) | 2022-02-28 | 0000-00-00 | No | No | Current |
| 71335-1641-3 | 71335164103 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1641-3) | 2022-02-28 | 0000-00-00 | No | No | Current |
| 71335-1641-4 | 71335164104 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1641-4) | 2022-02-28 | 0000-00-00 | No | No | Current |
| 71335-1641-5 | 71335164105 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1641-5) | 2022-02-28 | 0000-00-00 | No | No | Current |
| 71335-1641-6 | 71335164106 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1641-6) | 2022-02-28 | 0000-00-00 | No | No | Current |