Triamterene and Hydrochlorothiazide
- Product NDC
- 51655-631
- 11-digit product format
- 516550631
- Labeler code
- 51655
- Product ID
- 51655-631_d47908e0-6361-3320-e053-2995a90a6c22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA071851
- Marketing category
- ANDA
- Marketing start
- 2020-05-18
- Marketing end
- 0000-00-00
- Substance
- TRIAMTERENE; HYDROCHLOROTHIAZIDE
- Active strength
- 75 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-631-26 | Triamterene and Hydrochlorothiazide | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-631 | TRIAMTERENE AND HYDROCHLOROTHIAZIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 3 | Legacy NDC, 1 package rows | 20231115_ada10dd4-72e2-13b5-e053-2a95a90a8cfd.zip |
| 51655-631 | TRIAMTERENE AND HYDROCHLOROTHIAZIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 1 | Legacy NDC | 20150319_f2d5ec5e-9fd0-4f0e-aded-5a01b67e538b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51655-631-26 | 51655063126 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-631-26) | 90 tablet | 2020-05-18 | 0000-00-00 | No | No | Current |