Amlodipine and olmesartan medoxomil
- Product NDC
- 70771-1188
- 11-digit product format
- 707711188
- Labeler code
- 70771
- Product ID
- 70771-1188_adc1edc9-9897-4ba0-a14d-08c8d29f9369
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA207771
- Marketing category
- ANDA
- Marketing start
- 2018-01-04
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- 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 |
|---|
| 70771-1188-0 | 70771118800 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1188-0) | | 2018-01-04 | 0000-00-00 | No | No | Current |
| 70771-1188-1 | 70771118801 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1188-1) | | 2018-01-04 | 0000-00-00 | No | No | Current |
| 70771-1188-3 | 70771118803 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1188-3) | | 2018-01-04 | 0000-00-00 | No | No | Current |
| 70771-1188-4 | 70771118804 | 10 BLISTER PACK in 1 CARTON (70771-1188-4) > 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1188-2) | 10 blister pack | 2018-01-04 | 0000-00-00 | No | No | Current |
| 70771-1188-5 | 70771118805 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1188-5) | | 2018-01-04 | 0000-00-00 | No | No | Current |
| 70771-1188-9 | 70771118809 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1188-9) | | 2018-01-04 | 0000-00-00 | No | No | Current |