NDC 70985-021 - Oxybutynin Chloride Extended Release
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70985-021
- Package NDCs from labels
- 70985-021-01, 70985-021-02
- Manufacturer
- Drug Ocean LLC | Unique Pharmaceutical Laboratories
- Effective date
- 2023-10-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Oxybutynin Chloride - Drug Ocean LLC | Unique Pharmaceutical Laboratories | Drug Ocean LLC | Unique Pharmaceutical Laboratories | 2023-10-17 | HUMAN PRESCRIPTION DRUG LABEL |