atorvastatin calcium
- Product NDC
- 68645-591
- 11-digit product format
- 686450591
- Labeler code
- 68645
- Product ID
- 68645-591_a89e46e9-689a-4701-8289-559ef0459397
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atorvastatin calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA209912
- Marketing category
- ANDA
- Marketing start
- 2018-06-18
- Marketing end
- 2021-06-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68645-591-54 | 68645059154 | 30 TABLET in 1 BOTTLE (68645-591-54) | 30 tablet | 2018-06-18 | 2021-06-30 | No | No | Current |