NDC 50111-456 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC50111-456
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA071655
- Marketed since
- September 30, 1990
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 50111-456-01 | 100 TABLET in 1 BOTTLE (50111-456-01) | Sep 30, 1990 |
| 50111-456-02 | 500 TABLET in 1 BOTTLE (50111-456-02) | Sep 30, 1990 |
| 50111-456-03 | 1000 TABLET in 1 BOTTLE (50111-456-03) | Sep 30, 1990 |
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