ATORVASTATIN CALCIUM
- Product NDC
- 68645-459
- 11-digit product format
- 686450459
- Labeler code
- 68645
- Product ID
- 68645-459_5fac3606-5a05-4b01-8fb9-878444bfffeb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- NDA020702
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2011-11-30
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68645-459-54 | 68645045954 | 30 TABLET, FILM COATED in 1 BOTTLE (68645-459-54) | 2011-11-30 | 2021-06-30 | No | No | Current |