NDC Product
Human Prescription DrugOxybutynin Chloride NDC 16729-317
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for OxyBUTYnin chloride 15 mg 24HR Extended Release Oral Tablet (RxCUI 863628). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.
Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.
Manufacturer Quick Index
Found 44 manufactured products
Accord Healthcare, Inc.
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 16729-318
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 16729-319
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advagen Pharma Limited
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 72888-030
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 72888-031
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 72888-032
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 27241-155
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 27241-156
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 27241-157
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals LLC
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 65162-371
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 65162-372
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 65162-373
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 43353-282
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 43353-284
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 43353-322
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 42291-633
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 42291-634
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 42291-635
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 50268-627
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 50268-628
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 50268-629
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chartwell RX, LLC
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 62135-507
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 62135-508
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 62135-509
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Coupler LLC
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 67046-1600
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 62175-270
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 62175-271
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 62175-272
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Marlex Pharmaceuticals Inc
NDC Product
Oxybutynin Chloride NDC 10135-609
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Oxybutynin Chloride NDC 10135-610
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Oxybutynin Chloride NDC 10135-611
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Physicians Total Care, Inc.
NDC Product
Ditropan Xl NDC 54868-4502
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Ditropan Xl NDC 54868-4610
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Ditropan Xl NDC 54868-4835
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Oxybutynin Chloride NDC 54868-5743
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 64980-209
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 64980-210
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride Extended Release NDC 64980-211
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugOxybutynin NDC 70771-1086
- Generic Name
- Oxybutynin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin NDC 70771-1087
- Generic Name
- Oxybutynin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin NDC 70771-1088
- Generic Name
- Oxybutynin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugOxybutynin NDC 68382-255
- Generic Name
- Oxybutynin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin NDC 68382-256
- Generic Name
- Oxybutynin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin NDC 68382-257
- Generic Name
- Oxybutynin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
