Hydrochlorothiazide
- Product NDC
- 69367-123
- 11-digit product format
- 693670123
- Labeler code
- 69367
- Product ID
- 69367-123_734036ca-cbe2-4552-a009-c70bb33af804
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- ANDA203018
- Marketing category
- ANDA
- Marketing start
- 2016-02-01
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 mg/50mg
- 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 |
|---|
| 69367-123-04 | 69367012304 | 100 mg in 1 BOTTLE (69367-123-04) | 100 mg | 2016-02-01 | 0000-00-00 | No | No | Current |
| 69367-123-07 | 69367012307 | 1000 mg in 1 BOTTLE (69367-123-07) | 1000 mg | 2016-02-01 | 0000-00-00 | No | No | Current |