NDC 72789-049 – Oxybutynin chloride
Oxybutynin Chloride 10 mg/1 · Tablet, Extended Release · Oral
Product NDC72789-049
Product details
- Brand name
- Oxybutynin chloride
- Generic name
- Oxybutynin chloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207138
- Marketed since
- December 20, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 10 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72789-049-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-049-90) | Jan 28, 2020 |
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