Triamterene and Hydrochlorothiazide
- Product NDC
- 68788-9793
- 11-digit product format
- 687889793
- Labeler code
- 68788
- Product ID
- 68788-9793_18d5f8ec-1702-47c0-a827-8218c394233d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals
- Application
- NDA019129
- Marketing category
- NDA
- Marketing start
- 2012-04-30
- Marketing end
- 0000-00-00
- Substance
- TRIAMTERENE; HY
- Active strength
- 38 mg/1; mg/1
- Pharmacologic classes
- Decreased Renal
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record