bisoprolol fumarate and hydrochlorothiazide
- Product NDC
- 63629-7150
- 11-digit product format
- 636297150
- Labeler code
- 63629
- Product ID
- 63629-7150_59c39f58-2bae-42c6-ac7a-f181bc705122
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bisoprolol fumarate and hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079106
- Marketing category
- ANDA
- Marketing start
- 2010-10-12
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; BISOPROLOL FUMARATE
- Active strength
- 6 mg/1; mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7150-1 | 63629715001 | 30 TABLET in 1 BOTTLE (63629-7150-1) | 30 tablet | 2016-12-08 | 0000-00-00 | No | No | Current |