NDC product
Fosinopril Sodium and Hydrochlorothiazide
NDC 69097-972 · CIPLA USA INC.
Key facts
| Product NDC | 69097-972 |
|---|---|
| Proprietary name | Fosinopril Sodium and Hydrochlorothiazide |
| Nonproprietary name | Fosinopril Sodium and Hydrochlorothiazide |
| Substances | FOSINOPRIL SODIUM, HYDROCHLOROTHIAZIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | CIPLA USA INC. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA090228 |
| Pharmacologic classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
| Marketing start | Jul 24, 2020 |
| 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: