Excluded / Inactive
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for OXcarbazepine 300 mg Oral Tablet (RxCUI 312137). 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 94 manufactured products
ANI Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 62559-220
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 62559-221
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 62559-222
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
ASCLEMED USA INC.
NDC Product
Human Prescription DrugOxcarbazepine NDC 87063-208
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advagen Pharma Limited
NDC Product
Human Prescription DrugOxcarbazepine NDC 72888-087
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72888-088
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72888-089
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advagen Pharma Ltd.
NDC Product
Human Prescription DrugOxcarbazepine NDC 72888-460
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72888-461
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72888-462
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aidarex Pharmaceuticals LLC
NDC Product
Oxcarbazepine NDC 33261-684
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Oxcarbazepine NDC 33261-841
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Oxcarbazepine NDC 33261-842
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
American Health Packaging
NDC Product
Human Prescription DrugOxcarbazepine NDC 60687-711
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 60687-722
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 60687-733
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugOxcarbazepine NDC 50268-679
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 50268-680
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 50268-681
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Breckenridge Pharmaceutical, Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 51991-053
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 51991-054
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 51991-055
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 51991-292
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 51991-293
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 51991-294
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugOxcarbazepine NDC 63629-9186
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 71335-0090
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 71335-2548
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72162-1594
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 31722-023
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 31722-024
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 31722-025
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cardinal Health 107, LLC
NDC Product
Human Prescription DrugOxcarbazepine NDC 55154-2138
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 55154-2139
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 55154-4320
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 55154-4323
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Coupler LLC
NDC Product
Human Prescription DrugOxcarbazepine NDC 67046-0868
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 67046-1640
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 67046-2084
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
DIRECT RX
NDC Product
Trileptal NDC 61919-569
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
Glenmark Pharmaceuticals Inc., USA
NDC Product
Human Prescription DrugOxcarbazepine NDC 68462-137
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 68462-138
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 68462-139
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 60429-061
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 60429-062
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 60429-063
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7262
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7263
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7264
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7593
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7594
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7595
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugOxcarbazepine NDC 0615-8447
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0615-8448
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0615-8567
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0615-8634
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0615-8635
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0615-8636
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar RxLLC
NDC Product
Human Prescription DrugOxcarbazepine NDC 72603-271
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72603-272
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugTrileptal NDC 0078-0337
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTrileptal NDC 0078-0357
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTrileptal NDC 0078-0456
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTrileptal NDC 0078-0457
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Physicians Total Care, Inc.
NDC Product
Trileptal NDC 54868-4836
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Trileptal NDC 54868-4837
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Oxcarbazepine NDC 54868-5830
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Oxcarbazepine NDC 54868-6073
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Oxcarbazepine NDC 54868-6129
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Proficient Rx LP
NDC Product
Human Prescription DrugOxcarbazepine NDC 82804-209
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugOxcarbazepine NDC 70518-2276
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 70518-2370
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 70518-3237
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 70518-3921
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 70518-4663
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rebel Distributors Corp
NDC Product
Oxcarbazepine NDC 21695-862
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Oxcarbazepine NDC 21695-863
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Oxcarbazepine NDC 21695-864
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 62756-183
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 62756-184
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 62756-185
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Umedica Laboratories USA Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 60290-067
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 60290-068
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 60290-069
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
XLCare Pharmaceuticals Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 72865-283
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72865-284
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72865-285
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugOxcarbazepine NDC 70771-1842
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 70771-1843
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 70771-1844
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Pharmaceuticals (USA) Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 68382-691
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 68382-692
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 68382-693
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
