Hydrochlorothiazide
- Product NDC
- 82804-972
- 11-digit product format
- 828040972
- Labeler code
- 82804
- Product ID
- 82804-972_4c1a2fb9-133d-4bd5-a336-e47d54f22c97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA087059
- Marketing category
- ANDA
- Marketing start
- 2020-09-25
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0J48LPH2TH | HYDROCHLOROTHIAZIDE | 58-93-5 | HYDROCHLOROTHIAZIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-972-00 | 82804097200 | 100 TABLET in 1 BOTTLE (82804-972-00) | 100 tablet | 2025-02-13 | No | No | Historical |
| 82804-972-11 | 82804097211 | 1000 TABLET in 1 BOTTLE (82804-972-11) | 1000 tablet | 2025-02-13 | No | No | Historical |
| 82804-972-30 | 82804097230 | 30 TABLET in 1 BOTTLE (82804-972-30) | 30 tablet | 2025-02-13 | No | No | Historical |
| 82804-972-55 | 82804097255 | 500 TABLET in 1 BOTTLE (82804-972-55) | 500 tablet | 2025-02-13 | No | No | Historical |
| 82804-972-60 | 82804097260 | 60 TABLET in 1 BOTTLE (82804-972-60) | 60 tablet | 2025-02-13 | No | No | Historical |
| 82804-972-72 | 82804097272 | 120 TABLET in 1 BOTTLE (82804-972-72) | 120 tablet | 2025-02-13 | No | No | Historical |
| 82804-972-90 | 82804097290 | 90 TABLET in 1 BOTTLE (82804-972-90) | 90 tablet | 2025-02-13 | No | No | Historical |