Atorvastatin Calcium
- Product NDC
- 43063-487
- 11-digit product format
- 430630487
- Labeler code
- 43063
- Product ID
- 43063-487_e6893d2a-f937-5793-e053-2a95a90a3093
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA091624
- Marketing category
- ANDA
- Marketing start
- 2013-04-05
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-487-90 | 43063048790 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-487-90) | 2013-04-30 | 0000-00-00 | No | No | Current |