NDC 67296-2335 – oxybutynin
Oxybutynin Chloride 5 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC67296-2335
Product details
- Brand name
- oxybutynin
- Generic name
- oxybutynin
- Labeler
- Redpharm Drug
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202332
- Marketed since
- August 10, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 67296-2335-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-2335-3) | Aug 10, 2017 |
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