NDC 72789-417 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC72789-417
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209025
- Marketed since
- February 1, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 5 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72789-417-30 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-417-30) | Aug 18, 2025 |
| 72789-417-90 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-417-90) | Jun 21, 2024 |
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