NDC 0832-0038 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC0832-0038
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074625
- Marketed since
- November 7, 2011
- Marketing end
- December 31, 2028
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 5 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0832-0038-00 | 100 TABLET in 1 BOTTLE (0832-0038-00) | Nov 7, 2011 |
| 0832-0038-10 | 1000 TABLET in 1 BOTTLE (0832-0038-10) | Nov 7, 2011 |
| 0832-0038-50 | 500 TABLET in 1 BOTTLE (0832-0038-50) | Nov 7, 2011 |
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