NDC 64980-679 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC64980-679
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- RISING PHARMA HOLDINGS, INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209025
- Marketed since
- April 27, 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 |
|---|---|---|
| 64980-679-01 | 100 TABLET in 1 BOTTLE (64980-679-01) | Jul 18, 2026 |
| 64980-679-10 | 1000 TABLET in 1 BOTTLE (64980-679-10) | Apr 27, 2026 |
| 64980-679-50 | 500 TABLET in 1 BOTTLE (64980-679-50) | Apr 27, 2026 |
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