Olmesartan Medoxomil and Hydrochlorothiazide
- Product NDC
- 63629-7278
- 11-digit product format
- 636297278
- Labeler code
- 63629
- Product ID
- 63629-7278_b4395932-291d-4845-ac86-a3961d1b94da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200532
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- 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
- 2021-12-31
- 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 |
|---|
| 63629-7278-1 | 63629727801 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7278-1) | 2017-05-08 | 0000-00-00 | No | No | Current |
| 63629-7278-2 | 63629727802 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-7278-2) | 2017-05-08 | 0000-00-00 | No | No | Current |
| 63629-7278-3 | 63629727803 | 28 TABLET, FILM COATED in 1 BOTTLE (63629-7278-3) | 2017-05-08 | 0000-00-00 | No | No | Current |