Atorvastatin Calcium
- Product NDC
- 70518-3461
- 11-digit product format
- 705183461
- Labeler code
- 70518
- Product ID
- 70518-3461_e4b56728-6aca-a30e-e053-2a95a90a377c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076477
- Marketing category
- ANDA
- Marketing start
- 2022-07-25
- 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 |
|---|
| 70518-3461-0 | 70518346100 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3461-0) | 2022-07-25 | 0000-00-00 | No | No | Current |