Triamterene and Hydrochlorothiazide
- Product NDC
- 50090-1271
- 11-digit product format
- 500901271
- Labeler code
- 50090
- Product ID
- 50090-1271_a9008db1-7cce-4b28-a624-84b7083b18f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071251
- Marketing category
- ANDA
- Marketing start
- 2009-09-21
- 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 |
|---|
| 50090-1271-0 | 50090127100 | 30 TABLET in 1 BOTTLE, PLASTIC (50090-1271-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1271-1 | 50090127101 | 100 TABLET in 1 BOTTLE, PLASTIC (50090-1271-1) | 100 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1271-2 | 50090127102 | 90 TABLET in 1 BOTTLE, PLASTIC (50090-1271-2) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |