Hydrochlorothiazide
- Product NDC
- 55154-1483
- 11-digit product format
- 551541483
- Labeler code
- 55154
- Product ID
- 55154-1483_3ebc6562-ce2c-4fdc-97b9-008695fda859
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2007-06-28
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-1483-0 | 55154148300 | 10 BLISTER PACK in 1 BAG (55154-1483-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2007-06-28 | 0000-00-00 | No | No | Current |