NDC product
Triamterene and Hydrochlorothiazide
NDC 0781-2074 · Sandoz Inc
Key facts
| Product NDC | 0781-2074 |
|---|---|
| Proprietary name | Triamterene and Hydrochlorothiazide |
| Nonproprietary name | Triamterene and Hydrochlorothiazide |
| Substances | TRIAMTERENE, HYDROCHLOROTHIAZIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Sandoz Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA074821 |
| Pharmacologic classes | Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS] |
| Marketing start | Jun 5, 1997 |
| Listing certified through | Dec 31, 2027 |
At a glance
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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: