NDC product
Losartan Potassium and Hydrochlorothiazide
NDC 0093-7369 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0093-7369 |
|---|---|
| Proprietary name | Losartan Potassium and Hydrochlorothiazide |
| Nonproprietary name | Losartan Potassium and Hydrochlorothiazide |
| Substances | LOSARTAN POTASSIUM, HYDROCHLOROTHIAZIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA077157 |
| Pharmacologic classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
| Marketing start | Apr 6, 2010 |
| Listing certified through | Dec 31, 2027 |
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: