NDC product
Oxybutynin Chloride
NDC 23155-810 · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Key facts
| Product NDC | 23155-810 |
|---|---|
| Proprietary name | Oxybutynin Chloride |
| Nonproprietary name | Oxybutynin Chloride |
| Substances | OXYBUTYNIN CHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA208165 |
| Pharmacologic classes | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
| Marketing start | Jan 31, 2022 |
| Marketing end | Aug 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