NDC 62175-272 – Oxybutynin Chloride Extended Release
Oxybutynin Chloride 15 mg/1 · Tablet, Extended Release · Oral
Product NDC62175-272
Product details
- Brand name
- Oxybutynin Chloride Extended Release
- Generic name
- Oxybutynin Chloride
- Labeler
- Lannett Company, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078503
- Marketed since
- March 1, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 15 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 62175-272-37 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-272-37) | Mar 1, 2009 |
| 62175-272-41 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-272-41) | Mar 1, 2009 |
Recalls mentioning this NDC
- D-0996-2019 Mar 20, 2019 · Class III
Failed Dissolution Specifications
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