NDC product
Amiloride Hydrochloride and Hydrochlorothiazide
NDC 0555-0483 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0555-0483 |
|---|---|
| Proprietary name | Amiloride Hydrochloride and Hydrochlorothiazide |
| Nonproprietary name | Amiloride Hydrochloride and Hydrochlorothiazide |
| Substances | AMILORIDE HYDROCHLORIDE, HYDROCHLOROTHIAZIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA071111 |
| Pharmacologic classes | Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS] |
| Marketing start | Dec 1, 1989 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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: