Triamterene and Hydrochlorothiazide
- Product NDC
- 35356-974
- 11-digit product format
- 353560974
- Labeler code
- 35356
- Product ID
- 35356-974_79ee2a8b-8431-4af3-b666-e700852ae31d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA074821
- Marketing category
- ANDA
- Marketing start
- 1997-06-05
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; TRIAMTERENE
- Active strength
- 25 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
- 2022-12-31
- 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 |
|---|
| 35356-974-90 | 35356097490 | 90 CAPSULE in 1 BOTTLE (35356-974-90) | 90 capsule | 2021-03-26 | 0000-00-00 | No | No | Current |