Olmesartan Medoxomil and Hydrochlorothiazide
- Product NDC
- 71335-0203
- 11-digit product format
- 713350203
- Labeler code
- 71335
- Product ID
- 71335-0203_de0cb1c2-df4e-41b0-85fd-d2e0f7633aa0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil-hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021532
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-10-26
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
- Active strength
- 13 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
- 2023-12-31
- 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 |
|---|
| 71335-0203-1 | 71335020301 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0203-1) | 2016-10-26 | 0000-00-00 | No | No | Current |
| 71335-0203-2 | 71335020302 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0203-2) | 2016-10-26 | 0000-00-00 | No | No | Current |
| 71335-0203-3 | 71335020303 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0203-3) | 2016-10-26 | 0000-00-00 | No | No | Current |