NDC 69315-182 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC69315-182
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- Leading Pharma, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA212798
- Marketed since
- November 1, 2019
- 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 |
|---|---|---|
| 69315-182-01 | 100 TABLET in 1 BOTTLE (69315-182-01) | Nov 1, 2019 |
| 69315-182-05 | 500 TABLET in 1 BOTTLE (69315-182-05) | Nov 1, 2019 |
| 69315-182-10 | 1000 TABLET in 1 BOTTLE (69315-182-10) | Nov 1, 2019 |
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