NDC 64980-210 – Oxybutynin Chloride Extended Release
Oxybutynin Chloride 10 mg/1 · Tablet, Extended Release · Oral
Product NDC64980-210
Product details
- Brand name
- Oxybutynin Chloride Extended Release
- Generic name
- Oxybutynin Chloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA206121
- Marketed since
- September 27, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 10 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 64980-210-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-210-01) | Sep 27, 2016 |
| 64980-210-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-210-05) | Mar 29, 2022 |
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