Amlodipine and atorvastatin
- Product NDC
- 70771-1460
- 11-digit product format
- 707711460
- Labeler code
- 70771
- Product ID
- 70771-1460_a4beebf9-4f71-45f0-8707-9273c8f02097
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and atorvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA207762
- Marketing category
- ANDA
- Marketing start
- 2019-05-30
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1460-1 | 70771146001 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1460-1) | | 2019-05-30 | 0000-00-00 | No | No | Current |
| 70771-1460-3 | 70771146003 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1460-3) | | 2019-05-30 | 0000-00-00 | No | No | Current |
| 70771-1460-4 | 70771146004 | 10 BLISTER PACK in 1 CARTON (70771-1460-4) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2019-05-30 | 0000-00-00 | No | No | Current |
| 70771-1460-9 | 70771146009 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1460-9) | | 2019-05-30 | 0000-00-00 | No | No | Current |