Oxybutynin Chloride
- Product NDC
- 71610-860
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA075079
- Marketing category
- ANDA
- Substance
- OXYBUTYNIN CHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-860-30 | 30 TABLET in 1 BOTTLE (71610-860-30) | 2024-10-10 | | No | Historical |
| 71610-860-53 | 60 TABLET in 1 BOTTLE (71610-860-53) | 2024-10-10 | | No | Historical |
| 71610-860-60 | 90 TABLET in 1 BOTTLE (71610-860-60) | 2024-10-10 | | No | Historical |
| 71610-860-80 | 180 TABLET in 1 BOTTLE (71610-860-80) | 2024-10-10 | | No | Historical |