Hydrochlorothiazide 69367-0219
Product NDC
69367-0219- Manufacturer
- Westminster Pharmaceuticals, Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 7, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA203561
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Increased Diuresis [PE]Thiazide Diuretic [EPC]
Packaging Options(3)
100 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-01)
500 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-05)
1000 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-10)