Atorvastatin Calcium
- Product NDC
- 62175-897
- 11-digit product format
- 621750897
- Labeler code
- 62175
- Product ID
- 62175-897_e20ad87d-3bf3-4d7d-a014-70dc5ef98e7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lannett Company, 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 |
|---|
| 62175-897-41 | 62175089741 | 500 TABLET, FILM COATED in 1 BOTTLE (62175-897-41) | 2013-04-05 | 0000-00-00 | No | No | Current |
| 62175-897-44 | 62175089744 | 2500 TABLET, FILM COATED in 1 BOTTLE (62175-897-44) | 2013-04-05 | 0000-00-00 | No | No | Current |
| 62175-897-46 | 62175089746 | 90 TABLET, FILM COATED in 1 BOTTLE (62175-897-46) | 2013-04-05 | 0000-00-00 | No | No | Current |