Triamterene hydrochlorothiazide
- Product NDC
- 43063-442
- 11-digit product format
- 430630442
- Labeler code
- 43063
- Product ID
- 43063-442_a900c99c-99f1-f63b-e053-2a95a90a872d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA072011
- Marketing category
- ANDA
- Marketing start
- 1988-06-17
- Marketing end
- 2020-11-30
- Substance
- TRIAMTERENE; HYDROCHLOROTHIAZIDE
- Active strength
- 75 mg/1; mg/1
- Pharmacologic classes
- Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record