Amlodipine and olmesartan medoxomil
- Product NDC
- 59746-529
- 11-digit product format
- 597460529
- Labeler code
- 59746
- Product ID
- 59746-529_660f89b1-ff32-4d61-aa48-56d9e6c15dce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Application
- ANDA207450
- Marketing category
- ANDA
- Marketing start
- 2017-05-15
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 59746-529-01 | 59746052901 | 100 TABLET, FILM COATED in 1 BOTTLE (59746-529-01) | 2017-05-15 | 0000-00-00 | No | No | Current |
| 59746-529-10 | 59746052910 | 1000 TABLET, FILM COATED in 1 BOTTLE (59746-529-10) | 2017-05-15 | 0000-00-00 | No | No | Current |
| 59746-529-30 | 59746052930 | 30 TABLET, FILM COATED in 1 BOTTLE (59746-529-30) | 2017-05-15 | 0000-00-00 | No | No | Current |
| 59746-529-90 | 59746052990 | 90 TABLET, FILM COATED in 1 BOTTLE (59746-529-90) | 2017-05-15 | 0000-00-00 | No | No | Current |