NDC 65162-371 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet, Extended Release · Oral
Product NDC65162-371
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204010
- Marketed since
- November 2, 2015
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 65162-371-03 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-371-03) | Nov 2, 2015 |
| 65162-371-09 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-371-09) | Nov 2, 2015 |
| 65162-371-10 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-371-10) | Nov 2, 2015 |
| 65162-371-50 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-371-50) | Nov 2, 2015 |
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