NDC 72888-032 – Oxybutynin Chloride
Oxybutynin Chloride 15 mg/1 · Tablet, Extended Release · Oral
Product NDC72888-032
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- Advagen Pharma Limited
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA214415
- Marketed since
- October 27, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 15 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72888-032-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-032-01) | Oct 27, 2020 |
| 72888-032-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-032-05) | Jul 10, 2024 |
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