Atorvastatin Calcium
- Product NDC
- 70934-201
- 11-digit product format
- 709340201
- Labeler code
- 70934
- Product ID
- 70934-201_b7def290-565e-7f4b-e053-2995a90abf2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA091650
- Marketing category
- ANDA
- Marketing start
- 2019-03-25
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 70934-201-90 | 70934020190 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-201-90) | 90 tablet | 2019-03-25 | 0000-00-00 | No | No | Current |