Excluded / Inactive
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for DULoxetine 20 mg Delayed Release Oral Capsule (RxCUI 596926). 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 137 manufactured products
A-S Medication Solutions
NDC Product
Duloxetine NDC 50090-4709
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugDuloxetine NDC 50090-6406
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 50090-6889
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 50090-7812
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0228-2890
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0228-2891
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0228-2892
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advanced Rx Pharmacy of Tennessee, LLC
NDC Product
Human Prescription DrugDuloxetine Dr NDC 80425-0311
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugDuloxetine NDC 27241-097
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 27241-098
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 27241-099
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 27241-164
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Inc.
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 62332-278
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 62332-279
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 62332-280
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Duloxetine Hydrochloride 20 Mg NDC 46708-128
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Duloxetine Hydrochloride 30 Mg NDC 46708-129
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Duloxetine Hydrochloride 60 Mg NDC 46708-130
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 46708-278
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 46708-279
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 46708-280
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Human Prescription DrugDuloxetine NDC 71610-401
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 71610-402
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 71610-739
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 71610-957
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ascend Laboratories, LLC
NDC Product
Human Prescription DrugDuloxetine NDC 67877-263
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 67877-264
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 67877-265
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Asclemed USA, Inc.
NDC Product
Human Prescription DrugDuloxetine NDC 76420-623
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 76420-633
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 76420-634
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 76420-636
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 59651-279
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 59651-280
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 59651-282
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
BluePoint Laboratories
NDC Product
Human Prescription DrugDuloxetine NDC 68001-570
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 68001-594
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 68001-595
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 68001-596
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Breckenridge Pharmaceutical, Inc.
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 51991-746
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 51991-747
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 51991-748
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 51991-750
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 63629-1990
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 71335-0165
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 71335-1964
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 71335-2624
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 71335-3062
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 72162-1597
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cadila Healthcare Limited
NDC Product
Duloxetine NDC 65841-774
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Duloxetine NDC 65841-775
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Duloxetine NDC 65841-776
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugDuloxetine NDC 31722-168
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 31722-169
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 31722-170
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Carilion Materials Management
NDC Product
Cymbalta NDC 68151-4734
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
Cipla USA Inc.
NDC Product
Duloxetine NDC 69097-297
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Duloxetine NDC 69097-298
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Duloxetine NDC 69097-299
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Coupler LLC
NDC Product
Duloxetine NDC 67046-1253
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
DIRECT RX
NDC Product
Duloxetine NDC 61919-422
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Duloxetine NDC 61919-636
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Direct_Rx
NDC Product
Duloxetine NDC 61919-422
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugDuloxetine D/r NDC 72189-634
- Generic Name
- Duloxetine D/r
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugCymbalta NDC 0002-3235
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCymbalta NDC 0002-3240
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCymbalta NDC 0002-3270
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 51407-817
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 51407-818
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 51407-819
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 60429-164
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Duloxetine Delayed-release NDC 60429-165
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Duloxetine Delayed-release NDC 60429-166
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
Inventia Healthcare Limited.
NDC Product
Human Prescription DrugDuloxetine NDC 49252-007
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 49252-008
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 49252-009
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lupin Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugDuloxetine NDC 68180-294
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 68180-295
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 68180-296
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 68180-297
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
MARKSANS PHARMA LIMITED
NDC Product
Human Prescription DrugDuloxetine NDC 25000-608
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 25000-609
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 25000-610
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 33342-160
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 33342-161
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 33342-162
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugDuloxetine NDC 0615-8494
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0615-8495
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0615-8496
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugDuloxetine NDC 68071-3979
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 68071-2711
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Physicians Total Care, Inc.
NDC Product
Cymbalta NDC 54868-5192
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Cymbalta NDC 54868-5215
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Cymbalta NDC 54868-5315
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
Preferred Pharmaceuticals Inc.
NDC Product
Duloxetine Delayed-release NDC 68788-6380
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 68788-7897
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugDuloxetine Delayed-release NDC 63187-720
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 71205-005
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 71205-525
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Qingdao BAHEAL Pharmaceutical Co., Ltd.
NDC Product
Human Prescription DrugDuloxetine NDC 70247-012
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 70247-013
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 70247-014
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Quallent Pharmaceuticals Health LLC
NDC Product
Human Prescription DrugDuloxetine NDC 82009-170
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 82009-171
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 82009-172
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 82009-173
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Quallent Pharmaceuticals Health, LLC
NDC Product
Human Prescription DrugDuloxetine NDC 82009-029
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 82009-030
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 82009-031
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 82009-032
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugDuloxetine NDC 70518-1139
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
RPK Pharmaceuticals, Inc.
NDC Product
Duloxetine NDC 53002-1503
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Rebel Distributors Corp
NDC Product
Cymbalta NDC 21695-657
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
ST. MARY'S MEDICAL PARK PHARMACY
NDC Product
Human Prescription DrugDuloxetine NDC 60760-759
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Solco Healthcare US, LLC
NDC Product
Human Prescription DrugDuloxetine NDC 43547-379
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 43547-380
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 43547-381
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugDuloxetine NDC 47335-381
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 47335-382
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 47335-383
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Unit Dose Services
NDC Product
Duloxetine Hydrochloride NDC 50436-2995
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Duloxetine Hydrochloride NDC 50436-2996
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Duloxetine Hydrochloride NDC 50436-2997
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Yaopharma Co., Ltd.
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 50771-201
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 50771-202
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine Hydrochloride NDC 50771-203
- Generic Name
- Duloxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugDuloxetine NDC 65841-799
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 65841-800
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 65841-801
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
medsource pharmaceuticals
NDC Product
Duloxetine Delayed-release NDC 45865-815
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive