Triamterene hydrochlorothiazide
- Product NDC
- 50090-3106
- 11-digit product format
- 500903106
- Labeler code
- 50090
- Product ID
- 50090-3106_38e0953d-c375-4582-8e84-3a0ff0548bdc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA072011
- Marketing category
- ANDA
- Marketing start
- 2017-04-20
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record