NDC 71335-1014 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC71335-1014
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209025
- Marketed since
- February 1, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 5 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1014-1 | 30 TABLET in 1 BOTTLE (71335-1014-1) | Nov 21, 2018 |
| 71335-1014-2 | 100 TABLET in 1 BOTTLE (71335-1014-2) | Aug 9, 2024 |
| 71335-1014-3 | 20 TABLET in 1 BOTTLE (71335-1014-3) | Aug 9, 2024 |
| 71335-1014-4 | 60 TABLET in 1 BOTTLE (71335-1014-4) | Aug 9, 2024 |
| 71335-1014-5 | 90 TABLET in 1 BOTTLE (71335-1014-5) | Aug 9, 2024 |
| 71335-1014-6 | 42 TABLET in 1 BOTTLE (71335-1014-6) | Aug 9, 2024 |
| 71335-1014-7 | 15 TABLET in 1 BOTTLE (71335-1014-7) | Aug 9, 2024 |
| 71335-1014-8 | 180 TABLET in 1 BOTTLE (71335-1014-8) | Aug 9, 2024 |
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