atorvastatin calcium
- Product NDC
- 70518-2635
- 11-digit product format
- 705182635
- Labeler code
- 70518
- Product ID
- 70518-2635_cc090f28-5878-8644-e053-2a95a90a9ae5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atorvastatin calcium, film coated
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209912
- Marketing category
- ANDA
- Marketing start
- 2020-03-18
- 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 |
|---|
| 70518-2635-0 | 70518263500 | 30 TABLET in 1 BLISTER PACK (70518-2635-0) | 30 tablet | 2020-03-18 | 0000-00-00 | No | No | Current |