Olmesartan Medoxomil and Hydrochlorothiazide
- Product NDC
- 57664-759
- 11-digit product format
- 576640759
- Labeler code
- 57664
- Product ID
- 57664-759_5784665f-83c5-4153-937a-61d0f1e2483b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil-hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- NDA021532
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-10-26
- Marketing end
- 0000-00-00
- Substance
- OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE
- Active strength
- 40 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57664-759-83 | 57664075983 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-759-83) | 2016-10-26 | 0000-00-00 | No | No | Current |
| 57664-759-99 | 57664075999 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-759-99) | 2016-10-26 | 0000-00-00 | No | No | Current |