olmesartan medoxomil
- Product NDC
- 68382-643
- 11-digit product format
- 683820643
- Labeler code
- 68382
- Product ID
- 68382-643_0fb52f36-690a-4321-a374-345bfacf74b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA205192
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Marketing end
- 0000-00-00
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 5 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 |
|---|
| 68382-643-01 | 68382064301 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-643-01) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 68382-643-05 | 68382064305 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-643-05) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 68382-643-06 | 68382064306 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-643-06) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 68382-643-10 | 68382064310 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-643-10) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 68382-643-16 | 68382064316 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-643-16) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 68382-643-77 | 68382064377 | 10 BLISTER PACK in 1 CARTON (68382-643-77) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-643-30) | 10 blister pack | 2017-04-24 | 0000-00-00 | No | No | Current |