NDC 50268-629 – Oxybutynin Chloride Extended Release
Oxybutynin Chloride 15 mg/1 · Tablet, Extended Release · Oral
Product NDC50268-629
Product details
- Brand name
- Oxybutynin Chloride Extended Release
- Generic name
- Oxybutynin Chloride
- Labeler
- AvPAK
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078503
- Marketed since
- May 25, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 15 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50268-629-13 | 30 BLISTER PACK in 1 BOX (50268-629-13) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-629-11) | May 25, 2012 |
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