Atorvastatin Calcium
- Product NDC
- 63629-4850
- 11-digit product format
- 636294850
- Labeler code
- 63629
- Product ID
- 63629-4850_bd7cb86a-9800-4ffc-942b-e2b5ec34000e
- 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
- 80 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4850-1 | 63629485001 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4850-1) | 2014-03-24 | 0000-00-00 | No | No | Current |
| 63629-4850-2 | 63629485002 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4850-2) | 2014-03-13 | 0000-00-00 | No | No | Current |
| 63629-4850-3 | 63629485003 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4850-3) | 2013-08-06 | 0000-00-00 | No | No | Current |
| 63629-4850-4 | 63629485004 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-4850-4) | 2022-02-08 | 0000-00-00 | No | No | Current |