Excluded / Inactive
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for BuPROPion HCl 150 mg 12HR Extended Release Oral Tablet (RxCUI 993518). 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 116 manufactured products
A-S Medication Solutions
NDC Product
Bupropion Hydrochloride (sr) NDC 50090-3453
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 50090-6353
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 50090-6871
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 50090-6872
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 50090-7422
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 50090-7423
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 0591-3540
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 0591-3541
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 0591-3542
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aidarex Pharmaceuticals LLC
NDC Product
Bupropion Hydrochloride Sr (sr) NDC 33261-449
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
American Health Packaging
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 68084-697
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 68084-708
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Bupropion Hydrochloride NDC 43353-538
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride NDC 43353-546
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride NDC 67544-299
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride Sr NDC 71610-570
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 71610-576
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 71610-582
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 71610-990
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 59651-846
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 59651-847
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 59651-848
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 63629-8473
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 71335-0135
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 71335-1702
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 71335-1837
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 71335-2457
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 72162-1529
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 31722-066
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 31722-067
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 31722-068
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cardinal Health 107, LLC
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 55154-0183
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cipla USA Inc.,
NDC Product
Human Prescription DrugBupropion Hydrochloride (sr) NDC 69097-877
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride (sr) NDC 69097-878
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride (sr) NDC 69097-879
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
DIRECT RX
NDC Product
Bupropion Hydrochloride NDC 61919-038
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride NDC 61919-063
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
NDC Product
Bupropion Hydrochloride Sr NDC 70934-225
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Denton Pharma, Inc. dba Northwind Pharmaceuticals
NDC Product
Bupropion Hydrochloride Sr NDC 70934-791
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
DirectRx
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 72189-349
- Generic Name
- Bupropion Hydrochloride Sr
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Direct_Rx
NDC Product
Bupropion Hydrochloride NDC 61919-063
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Bupropion Hydrochloride NDC 61919-136
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Dr. Reddy�s Laboratories Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43598-536
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43598-537
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43598-538
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43598-751
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43598-752
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43598-753
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Epic Pharma LLC
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 42806-410
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 42806-411
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 42806-415
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Epic Pharma, LLC
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 42806-424
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 42806-425
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 42806-426
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
GlaxoSmithKline LLC
NDC Product
Human Prescription DrugWellbutrin Sr NDC 0173-0135
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugWellbutrin Sr NDC 0173-0722
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugWellbutrin Sr NDC 0173-0947
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Granules Pharmaceuticals Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 70010-125
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 70010-126
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 70010-127
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
H.J. Harkins Company, Inc.
NDC Product
Bupropion Hydrochloride NDC 52959-806
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Liberty Pharmaceuticals, Inc.
NDC Product
Bupropion Hydrochloride NDC 0440-7200
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Major Pharmaceuticals
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 0904-7099
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 0904-7465
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 0615-8601
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 0615-8602
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northwind Health Company, LLC
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 51655-115
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion NDC 51655-357
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 82868-019
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Bupropion Hydrochloride Sr NDC 68071-1573
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 68071-2890
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43063-744
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43063-913
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Physicians Total Care, Inc.
NDC Product
Bupropion Hydrochloride Sr NDC 54868-4892
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride Sr NDC 54868-5377
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride Sr NDC 54868-6306
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 68788-8769
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Preferred Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 68788-7807
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 63187-052
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 63187-176
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 63187-178
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 63187-726
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 71205-550
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion NDC 71205-565
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 70518-4056
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 70518-4081
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
RPK Pharmaceuticals, Inc.
NDC Product
Bupropion Hydrochloride Sr NDC 53002-1345
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Radha Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 77771-174
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 77771-175
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 77771-176
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rebel Distributors Corp.
NDC Product
Bupropion Hydrochloride NDC 21695-019
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride NDC 21695-020
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride NDC 21695-295
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
RxChange Co.
NDC Product
Bupropion Hydrochloride NDC 33358-364
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
STAT RX USA LLC
NDC Product
Bupropion Hydrochloride NDC 16590-036
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride NDC 16590-038
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
ScieGen Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 50228-174
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 50228-175
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 50228-176
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Slate Run Pharmaceuticals, LLC
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 70436-058
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 70436-059
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 70436-060
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Solco Healthcare US LLC
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43547-288
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43547-289
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 43547-290
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 47335-736
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 47335-737
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 47335-738
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
TYA Pharmaceuticals
NDC Product
Bupropion Hydrochloride NDC 64725-0736
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride NDC 64725-0737
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Unit Dose Services
NDC Product
Bupropion NDC 50436-0289
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride Sr NDC 50436-3541
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Wockhardt Limited
NDC Product
Bupropion Hydrochloride (sr) NDC 55648-101
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride (sr) NDC 55648-105
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Bupropion Hydrochloride (sr) NDC 55648-107
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive