Triamterene and Hydrochlorothiazide
- Product NDC
- 70518-0875
- 11-digit product format
- 705180875
- Labeler code
- 70518
- Product ID
- 70518-0875_e285fec3-3d2e-7b7d-e053-2995a90a47c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071251
- Marketing category
- ANDA
- Marketing start
- 2017-11-29
- 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
- 2023-12-31
- 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 |
|---|
| 70518-0875-0 | 70518087500 | 30 TABLET in 1 BLISTER PACK (70518-0875-0) | 30 tablet | 2017-11-29 | 0000-00-00 | No | No | Current |