Atorvastatin Calcium
- Product NDC
- 68071-4472
- 11-digit product format
- 680714472
- Labeler code
- 68071
- Product ID
- 68071-4472_d6061620-04e5-34c6-e053-2a95a90a9ef1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA205300
- Marketing category
- ANDA
- Marketing start
- 2017-05-04
- 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 |
|---|
| 68071-4472-9 | 68071447209 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4472-9) | 2018-06-14 | 0000-00-00 | No | No | Current |