Hydrochlorothiazide
- Product NDC
- 53002-4972
- 11-digit product format
- 530024972
- Labeler code
- 53002
- Product ID
- 53002-4972_d8d17974-bd7b-4ddd-b4a5-808b041e39e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA083177
- Marketing category
- ANDA
- Marketing start
- 1973-01-12
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-4972-0 | 53002497200 | 100 TABLET in 1 BOTTLE (53002-4972-0) | 100 tablet | 2022-09-01 | 0000-00-00 | No | No | Current |
| 53002-4972-1 | 53002497201 | 10 TABLET in 1 BOTTLE (53002-4972-1) | 10 tablet | 2022-09-01 | 0000-00-00 | No | No | Current |
| 53002-4972-3 | 53002497203 | 30 TABLET in 1 BOTTLE (53002-4972-3) | 30 tablet | 2022-09-01 | 0000-00-00 | No | No | Current |