Olmesartan Medoxomil
- Product NDC
- 13668-250
- 11-digit product format
- 136680250
- Labeler code
- 13668
- Product ID
- 13668-250_e3a29777-823d-8511-e053-2995a90ab53c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA202375
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Marketing end
- 0000-00-00
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- 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 |
|---|
| 13668-250-05 | 13668025005 | 500 TABLET in 1 BOTTLE (13668-250-05) | 500 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 13668-250-30 | 13668025030 | 30 TABLET in 1 BOTTLE (13668-250-30) | 30 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 13668-250-74 | 13668025074 | 100 TABLET in 1 CARTON (13668-250-74) | 100 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 13668-250-90 | 13668025090 | 90 TABLET in 1 BOTTLE (13668-250-90) | 90 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |