ATORVASTATIN CALCIUM
- Product NDC
- 70518-1977
- 11-digit product format
- 705181977
- Labeler code
- 70518
- Product ID
- 70518-1977_eff84665-564d-7532-e053-2995a90ad3bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207687
- 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
- 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 |
|---|
| 70518-1977-0 | 70518197700 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1977-0) | 2019-03-25 | 0000-00-00 | No | No | Current |
| 70518-1977-1 | 70518197701 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1977-1) | 2019-03-25 | 0000-00-00 | No | No | Current |
| 70518-1977-2 | 70518197702 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1977-2) | 2019-06-26 | 0000-00-00 | No | No | Current |