NDC 68084-480 – Oxybutynin Chloride Extended Release
Oxybutynin Chloride 5 mg/1 · Tablet, Extended Release · Oral
Product NDC68084-480
Product details
- Brand name
- Oxybutynin Chloride Extended Release
- Generic name
- Oxybutynin Chloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078503
- Marketed since
- January 13, 2012
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 68084-480-01 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-480-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-480-11) | Jan 13, 2012 |
| 68084-480-65 | 50 BLISTER PACK in 1 CARTON (68084-480-65) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-480-11) | Feb 21, 2023 |
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