Triamterene and Hydrochlorothiazide
- Product NDC
- 68071-3080
- 11-digit product format
- 680713080
- Labeler code
- 68071
- Product ID
- 68071-3080_bdeb2d3e-947d-60bc-e053-2a95a90a1f23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA201407
- Marketing category
- ANDA
- Marketing start
- 2011-12-12
- 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 |
|---|
| 68071-3080-3 | 68071308003 | 30 CAPSULE in 1 BOTTLE (68071-3080-3) | 30 capsule | 2017-03-14 | 0000-00-00 | No | No | Current |
| 68071-3080-9 | 68071308009 | 90 CAPSULE in 1 BOTTLE (68071-3080-9) | 90 capsule | 2017-03-14 | 0000-00-00 | No | No | Current |