Triamterene and Hydrochlorothiazide
- Product NDC
- 63629-8191
- 11-digit product format
- 636298191
- Labeler code
- 63629
- Product ID
- 63629-8191_f0ab4a09-730b-433e-b129-04911acd5191
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071851
- Marketing category
- ANDA
- Marketing start
- 1993-09-23
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; TRIAMTERENE
- Active strength
- 50 mg/1; mg/1
- Pharmacologic classes
- Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-8191-1 | 63629819101 | 30 TABLET in 1 BOTTLE (63629-8191-1) | 30 tablet | 2019-08-02 | 0000-00-00 | No | No | Current |