NDC Product
Human Prescription DrugParoxetine NDC 50090-0850
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Paroxetine Hydrochloride, uniquely identified by the FDA Unique Ingredient Identifier (UNII) X2ELS050D8.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 110429-35-1 and the RxNorm Concept ID (RxCUI) 1298842. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
PAROXETINE HYDROCHLORIDE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
X2ELS050D8
The specific atomic composition represented as a molecular structure string.
InChIKey
2C19H20FNO3.2ClH.H2O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
MQZOATSIFWSKKT-OASXIEIISA-N Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
c12cc(OC[C@@H]3CNCC[C@H]3c4ccc(F)cc4)ccc1OCO2.Cl.O.c12cc(OC[C@@H]3CNCC[C@H]3c4ccc(F)cc4)ccc1OCO2.Cl
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Paroxetine Hydrochloride. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
FDA Official Name
PAROXETINE HYDROCHLORIDE
OF
Common Names & Synonyms
PAROXETINE HYDROCHLORIDE [ORANGE BOOK]
CN
PAROXETINE HYDROCHLORIDE [USP-RS]
CN
PAROXETINE HYDROCHLORIDE [VANDF]
CN
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
CN
PAROXETINE HYDROCHLORIDE HEMIHYDRATE [EP MONOGRAPH]
CN
PAROXETINE HYDROCHLORIDE HEMIHYDRATE [MI]
CN
PAROXETINE HYDROCHLORIDE HEMIHYDRATE [USP MONOGRAPH]
CN
PAROXETINE HYDROCHLORIDE HEMIHYDRATE [WHO-DD]
CN
PAROXETINE HYDROCHLORIDE HYDRATE
CN
PAROXETINE HYDROCHLORIDE HYDRATE [JAN]
CN
Brand / Trade Names
AROPAX
BN
DEROXAT
BN
PAXIL
BN
PAXIL CR
BN
SEROXAT
BN
Systematic Nomenclature
(-)-(3S,4R)-4-(P-FLUOROPHENYL)-3-((3,4-METHYLENEDIOXY)PHENOXY)-METHYL)PIPERIDINE HYDROCHLORIDE HEMIHYDRATE
SYS
Technical Codes
BRL29060A
CD
NDC Products Containing PAROXETINE HYDROCHLORIDE
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Note: Due to the high number of listings (181), only Active Listings are currently displayed.
Showing 131 active products
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 50090-1297
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
ANI Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugParoxetine NDC 70954-319
- Generic Name
- Paroxetine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advanced Rx Pharmacy of Tennessee, LLC
NDC Product
Human Prescription DrugParoxetine NDC 80425-0339
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Inc.
NDC Product
Human Prescription DrugParoxetine NDC 62332-767
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 62332-768
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Human Prescription DrugParoxetine NDC 46708-767
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 46708-768
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
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 43353-713
- Generic Name
- Paroxetine
- 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 71610-204
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 71610-243
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- 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
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
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
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
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
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
Bryant Ranch Prepack
NDC Product
Human Prescription DrugParoxetine NDC 63629-1840
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 63629-3349
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 63629-8527
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 71335-0544
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 71335-9650
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 72162-2358
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cadila Pharmaceuticals Limited
NDC Product
Human Prescription DrugParoxetine NDC 71209-094
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 71209-095
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 71209-096
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 31722-578
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chartwell RX, LLC
NDC Product
Human Prescription DrugParoxetine NDC 62135-425
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 62135-426
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 62135-427
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- 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
DIRECT RX
NDC Product
Human Prescription DrugParoxetine NDC 61919-513
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Direct_Rx
NDC Product
Human Prescription DrugParoxetine NDC 72189-492
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 62175-470
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 62175-471
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine Hydrochloride NDC 62175-472
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lupin Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugParoxetine NDC 68180-645
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68180-646
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68180-647
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Modavar Pharmaceuticals LLC
NDC Product
Human Prescription DrugParoxetine NDC 72241-029
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 72241-030
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 72241-031
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- 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
NDC Product
Human Prescription DrugParoxetine NDC 0615-8359
- 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 Pharamceuticals, Inc.
NDC Product
Human Prescription DrugParoxetine NDC 68071-2535
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugParoxetine NDC 68071-2835
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68071-3843
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugParoxetine NDC 68071-1740
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
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 55289-037
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
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 55289-972
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 72789-379
- 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
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
NDC Product
Human Prescription DrugParoxetine NDC 68788-7410
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68788-8777
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68788-8829
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Preferred Pharmaceuticals, Inc
NDC Product
Human Prescription DrugParoxetine NDC 68788-0797
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 68788-9074
- Generic Name
- Paroxetine Hydrochloride
- 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 63187-564
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 63187-927
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- 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
NDC Product
Human Prescription DrugParoxetine NDC 71205-527
- 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 70518-1253
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-1406
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-2376
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-2387
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-2465
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-2574
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-3430
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 70518-3518
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
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
Westminster Pharmaceuticals, LLC
NDC Product
Human Prescription DrugParoxetine NDC 69367-335
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 69367-336
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 69367-337
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
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 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
