NDC product
oxybutynin
NDC 0615-8219 · NCS HealthCare of KY, LLC dba Vangard Labs
Key facts
| Product NDC | 0615-8219 |
|---|---|
| Proprietary name | oxybutynin |
| Nonproprietary name | oxybutynin |
| Substances | OXYBUTYNIN CHLORIDE |
| Dosage form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | NCS HealthCare of KY, LLC dba Vangard Labs |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA202332 |
| Pharmacologic classes | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
| Marketing start | Aug 10, 2017 |
| 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: