Atorvastatin Calcium
- Product NDC
- 63629-0087
- 11-digit product format
- 636290087
- Labeler code
- 63629
- Product ID
- 63629-0087_c2c95ed8-d817-4c9b-9d85-f6ad9cf570e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205300
- Marketing category
- ANDA
- Marketing start
- 2017-05-04
- 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
- 2022-12-31
- 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 |
|---|
| 63629-0087-1 | 63629008701 | 1 TABLET, FILM COATED in 1 POUCH (63629-0087-1) | 2018-02-07 | 0000-00-00 | No | No | Current |