HYDROCHLOROTHIAZIDE
- Product NDC
- 50090-6372
- 11-digit product format
- 500906372
- Labeler code
- 50090
- Product ID
- 50090-6372_e25b6732-85b6-41a7-bda4-551c91e95407
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040702
- Marketing category
- ANDA
- Marketing start
- 2019-11-01
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 12.5 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 |
|---|
| 50090-6372-0 | 50090637200 | 30 TABLET in 1 BOTTLE (50090-6372-0) | 30 tablet | 2023-02-13 | No | No | Historical |
| 50090-6372-2 | 50090637202 | 100 TABLET in 1 BOTTLE (50090-6372-2) | 100 tablet | 2023-02-13 | No | No | Historical |
| 50090-6372-3 | 50090637203 | 90 TABLET in 1 BOTTLE (50090-6372-3) | 90 tablet | 2023-02-13 | No | No | Historical |