NDC product
Brimonidine Tartrate and Timolol Maleate
NDC 0781-7186 · Sandoz Inc
Key facts
| Product NDC | 0781-7186 |
|---|---|
| Proprietary name | Brimonidine Tartrate and Timolol Maleate |
| Nonproprietary name | Brimonidine Tartrate and Timolol Maleate |
| Substances | BRIMONIDINE TARTRATE, TIMOLOL MALEATE |
| Dosage form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Labeler | Sandoz Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA091087 |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Adrenergic beta-Antagonists [MoA], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Blocker [EPC] |
| Marketing start | Apr 13, 2022 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
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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: