ATORVASTATIN CALCIUM
- Product NDC
- 70518-1946
- 11-digit product format
- 705181946
- Labeler code
- 70518
- Product ID
- 70518-1946_d27d770b-bc02-5d82-e053-2995a90a7537
- 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
- 2019-03-11
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 10 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1946-0 | 70518194600 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1946-0) | 2019-03-11 | 0000-00-00 | No | No | Current |
| 70518-1946-1 | 70518194601 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1946-1) | 2019-04-30 | 0000-00-00 | No | No | Current |
| 70518-1946-2 | 70518194602 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1946-2) | 2021-12-03 | 0000-00-00 | No | No | Current |