Triamterene and Hydrochlorothiazide
- Product NDC
- 60760-535
- 11-digit product format
- 607600535
- Labeler code
- 60760
- Product ID
- 60760-535_9cbce27a-aec5-4828-e053-2a95a90a02e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene, Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA201407
- Marketing category
- ANDA
- Marketing start
- 2014-04-22
- 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
- 2021-12-31
- 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 |
|---|
| 60760-535-90 | 60760053590 | 90 CAPSULE in 1 BOTTLE, PLASTIC (60760-535-90) | 90 capsule | 2014-04-22 | 0000-00-00 | No | No | Current |