Excluded / Inactive
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for PARoxetine HCl 40 mg Oral Tablet (RxCUI 1738511). 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 125 manufactured products
A-S Medication Solutions
NDC Product
Paroxetine NDC 50090-0922
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
American Health Packaging
NDC Product
Human Prescription DrugParoxetine NDC 68084-044
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68084-045
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68084-046
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68084-047
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Human Prescription DrugParoxetine NDC 43353-544
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 43353-554
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 67544-492
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 71610-056
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 71610-992
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Apotex Corp
NDC Product
Human Prescription DrugPaxil NDC 60505-4517
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPaxil NDC 60505-4518
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPaxil NDC 60505-4519
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPaxil NDC 60505-4520
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Apotex Corp.
NDC Product
Human Prescription DrugParoxetine NDC 60505-0083
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 60505-0084
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 60505-0097
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 60505-0101
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Asclemed USA, Inc.
NDC Product
Human Prescription DrugParoxetine NDC 76420-716
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 76420-717
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 76420-718
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 76420-719
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Drug For Further Processing- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 65862-154
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 65862-155
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 65862-156
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 65862-157
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurolife Pharma LLC
NDC Product
Human Prescription DrugParoxetine NDC 13107-154
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-155
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-156
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-157
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugParoxetine NDC 50268-640
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Paroxetine NDC 50268-641
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 50268-642
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 50268-643
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Blenheim Pharmacal, Inc.
NDC Product
Paroxetine NDC 10544-433
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 10544-809
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Bryant Ranch Prepack
NDC Product
Human Prescription DrugParoxetine NDC 63629-3349
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Paroxetine NDC 71335-0603
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 71335-0675
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 71335-1046
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Paroxetine NDC 71335-1506
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugParoxetine NDC 72162-2358
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chartwell RX, LLC.
NDC Product
Human Prescription DrugParoxetine NDC 62135-541
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 62135-542
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 62135-543
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 62135-544
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Contract Pharmacy Services-PA
NDC Product
Paroxetine NDC 67046-530
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 67046-531
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 67046-532
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 67046-533
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
DIRECT RX
NDC Product
Human Prescription DrugParoxetine NDC 61919-513
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugParoxetine NDC 60429-734
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 60429-735
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 60429-736
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 60429-737
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugParoxetine NDC 0904-5676
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0904-5677
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Paroxetine NDC 0904-5678
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Paroxetine NDC 0904-5679
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugParoxetine NDC 0378-7001
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7002
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7003
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7004
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugParoxetine NDC 0615-7985
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0615-8173
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0615-8174
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar Rx LLC
NDC Product
Human Prescription DrugParoxetine NDC 16714-181
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 16714-182
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 16714-183
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 16714-184
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Paroxetine NDC 68071-4997
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Oxford Pharmaceuticals, LLC
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 69584-671
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 69584-672
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 69584-673
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 69584-674
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugParoxetine NDC 55289-053
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 72789-420
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Physicians Total Care, Inc.
NDC Product
Paroxetine NDC 54868-4817
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 54868-4937
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 54868-4938
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 54868-5080
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugParoxetine NDC 68788-6870
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugParoxetine NDC 63187-105
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 63187-190
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 63187-434
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 71205-198
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugParoxetine NDC 70518-0003
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-0993
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-1253
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rebel Distributors Corp
NDC Product
Paroxetine NDC 21695-101
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 21695-102
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 21695-103
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 21695-104
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Solco Healthcare US, LLC
NDC Product
Human Prescription DrugParoxetine NDC 43547-347
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 43547-348
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 43547-349
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 43547-350
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
State of Florida DOH Central Pharmacy
NDC Product
Paroxetine NDC 53808-0393
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0394
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0601
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0655
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0748
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0749
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0750
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0752
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0753
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0754
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Paroxetine NDC 53808-0756
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Yiling Pharmaceutical, Inc.
NDC Product
Human Prescription DrugParoxetine NDC 69117-0024
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 69117-0025
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 69117-0026
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 69117-0027
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugParoxetine NDC 65841-097
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 65841-098
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 65841-099
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 65841-601
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugParoxetine NDC 68382-001
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68382-097
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68382-098
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68382-099
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
