HYDROCHLOROTHIAZIDE
- Product NDC
- 0615-8450
- 11-digit product format
- 006158450
- Labeler code
- 0615
- Product ID
- 0615-8450_dffa477a-6ab3-4c52-aa0a-f11b90a00d0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA085182
- Marketing category
- ANDA
- Marketing start
- 2015-01-15
- 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 |
|---|
| 0615-8450-05 | 00615845005 | 15 TABLET in 1 BLISTER PACK (0615-8450-05) | 15 tablet | 2023-04-13 | No | No | Historical |
| 0615-8450-39 | 00615845039 | 30 TABLET in 1 BLISTER PACK (0615-8450-39) | 30 tablet | 2023-04-13 | No | No | Historical |