Triamterene and Hydrochlorothiazide
- Product NDC
- 63629-6712
- 11-digit product format
- 636296712
- Labeler code
- 63629
- Product ID
- 63629-6712_dc29307c-33f5-4dae-bdae-d0c6ca97f51c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA019129
- Marketing category
- NDA
- Marketing start
- 1996-09-16
- Marketing end
- 0000-00-00
- Substance
- TRIAMTERENE; HYDROCHLOROTHIAZIDE
- Active strength
- 38 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6712-1 | 63629671201 | 30 TABLET in 1 BOTTLE (63629-6712-1) | 30 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |