Triamterene and Hydrochlorothiazide
- Product NDC
- 51079-433
- 11-digit product format
- 510790433
- Labeler code
- 51079
- Product ID
- 51079-433_9e02f45a-8182-88bd-e053-2995a90ad9f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- NDA019129
- Marketing category
- NDA
- Marketing start
- 1998-10-26
- Marketing end
- 2021-08-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51079-433-20 | 51079043320 | 100 BLISTER PACK in 1 CARTON (51079-433-20) > 1 TABLET in 1 BLISTER PACK (51079-433-01) | 100 blister pack | 1998-10-26 | 2021-08-31 | No | No | Current |