Bisoprolol Fumarate and Hydrochlorothiazide
- Product NDC
- 70518-3333
- 11-digit product format
- 705183333
- Labeler code
- 70518
- Product ID
- 70518-3333_d5f2ae61-0716-3ec7-e053-2a95a90a1ad2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bisoprolol fumarate and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075768
- Marketing category
- ANDA
- Marketing start
- 2022-01-13
- Marketing end
- 0000-00-00
- Substance
- BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
- Active strength
- 3 mg/1; mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3333-0 | 70518333300 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3333-0) | 2022-01-13 | 0000-00-00 | No | No | Current |