NDC product
Timolol Maleate Ophthalmic Gel Forming Solution 0.5%
NDC 43598-748 · Dr. Reddy's Laboratories, Inc.
Key facts
| Product NDC | 43598-748 |
|---|---|
| Proprietary name | Timolol Maleate Ophthalmic Gel Forming Solution 0.5% |
| Nonproprietary name | Timolol Maleate Ophthalmic Gel Forming Solution 0.5% |
| Substances | TIMOLOL MALEATE |
| Dosage form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Labeler | Dr. Reddy's Laboratories, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA215733 |
| Pharmacologic classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
| Marketing start | Nov 15, 2022 |
| 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: