Atorvastatin Calcium
- Product NDC
- 68071-4835
- 11-digit product format
- 680714835
- Labeler code
- 68071
- Product ID
- 68071-4835_bb8ffb44-5468-9c05-e053-2a95a90adf18
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA209288
- Marketing category
- ANDA
- Marketing start
- 2018-12-23
- 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 |
|---|
| 68071-4835-6 | 68071483506 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-4835-6) | 2019-04-08 | 0000-00-00 | No | No | Current |