Atorvastatin calcium
- Product NDC
- 70934-823
- 11-digit product format
- 709340823
- Labeler code
- 70934
- Product ID
- 70934-823_d21bd1f9-2b0a-6270-e053-2995a90aefc5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA211933
- Marketing category
- ANDA
- Marketing start
- 2021-01-26
- 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 |
|---|
| 70934-823-90 | 70934082390 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-823-90) | 2021-01-26 | 0000-00-00 | No | No | Current |