NDC 71335-2121 – Oxybutynin Chloride Extended Release
Oxybutynin Chloride 10 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-2121
Product details
- Brand name
- Oxybutynin Chloride Extended Release
- Generic name
- Oxybutynin Chloride
- Labeler
- Bryant Ranch Prepack
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2121-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-1) | Jun 20, 2022 |
| 71335-2121-2 | 18 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-2) | Jun 20, 2022 |
| 71335-2121-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-3) | Jun 20, 2022 |
| 71335-2121-4 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-4) | Jun 20, 2022 |
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