NDC product
Triamterene and Hydrochlorothiazide
NDC 68788-7526 · Preferred Pharmaceuticals, Inc.
Key facts
| Product NDC | 68788-7526 |
|---|---|
| Proprietary name | Triamterene and Hydrochlorothiazide |
| Nonproprietary name | Triamterene and Hydrochlorothiazide |
| Substances | TRIAMTERENE, HYDROCHLOROTHIAZIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Preferred Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA073449 |
| Pharmacologic classes | Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS] |
| Marketing start | Sep 23, 1993 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
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About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: