NDC 23155-913 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC23155-913
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA211682
- Marketed since
- June 1, 2026
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 23155-913-01 | 100 TABLET in 1 BOTTLE, PLASTIC (23155-913-01) | Jun 1, 2026 |
| 23155-913-05 | 500 TABLET in 1 BOTTLE, PLASTIC (23155-913-05) | Jun 1, 2026 |
| 23155-913-10 | 1000 TABLET in 1 BOTTLE, PLASTIC (23155-913-10) | Jun 1, 2026 |
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