NDC 83939-0022 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC83939-0022
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- VERITYRX, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209823
- Marketed since
- November 15, 2017
- 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 |
|---|---|---|
| 83939-0022-1 | 1 TABLET in 1 POUCH (83939-0022-1) | Nov 3, 2025 |
| 83939-0022-2 | 50 POUCH in 1 BOX, UNIT-DOSE (83939-0022-2) / 1 TABLET in 1 POUCH | Nov 3, 2025 |
| 83939-0022-3 | 100 POUCH in 1 BOX, UNIT-DOSE (83939-0022-3) / 1 TABLET in 1 POUCH | Nov 3, 2025 |
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