FDA.reportPublic FDA data

PAROXETINE

Product NDC
60505-0084
Requested package NDC
60505-0084-9
11-digit product format
605050084
Labeler code
60505
Product ID
60505-0084_9cde2ef4-fd50-ed21-0628-cb6cd8a6153f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
paroxetine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Apotex Corp.
Application
ANDA075356
Marketing category
ANDA
Marketing start
2003-09-08
Substance
PAROXETINE HYDROCHLORIDE ANHYDROUS
Active strength
30 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage60505-008460505-0084-9DDiscontinued by firm2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A075356-001PAROXETINE HYDROCHLORIDEPAROXETINE HYDROCHLORIDEEQ 10MG BASETABLET / ORALAB2003-07-30
A075356-002PAROXETINE HYDROCHLORIDEPAROXETINE HYDROCHLORIDEEQ 20MG BASETABLET / ORALAB2003-07-30
A075356-003PAROXETINE HYDROCHLORIDEPAROXETINE HYDROCHLORIDEEQ 30MG BASETABLET / ORALAB2003-07-30
A075356-004PAROXETINE HYDROCHLORIDEPAROXETINE HYDROCHLORIDEEQ 40MG BASETABLET / ORALAB2003-07-30

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 4 matching rows.

Application-product, TE code table
Application-productTE code
A075356-001AB
A075356-002AB
A075356-003AB
A075356-004AB

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-01 22:54:322026-06A075356-001PAROXETINE HYDROCHLORIDEEQ 10MG BASETABLET / ORALAB2003-07-30a50c72e98297…
2026-08-01 22:54:322026-06A075356-002PAROXETINE HYDROCHLORIDEEQ 20MG BASETABLET / ORALAB2003-07-30a50c72e98297…
2026-08-01 22:54:322026-06A075356-003PAROXETINE HYDROCHLORIDEEQ 30MG BASETABLET / ORALAB2003-07-30a50c72e98297…
2026-08-01 22:54:322026-06A075356-004PAROXETINE HYDROCHLORIDEEQ 40MG BASETABLET / ORALAB2003-07-30a50c72e98297…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-08-01 22:54:322026-06A075356-001AB1a50c72e98297…
2026-08-01 22:54:322026-06A075356-002AB1a50c72e98297…
2026-08-01 22:54:322026-06A075356-003AB1a50c72e98297…
2026-08-01 22:54:322026-06A075356-004AB1a50c72e98297…

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 10 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PAROXETINEPAROXETINE HYDROCHLORIDEREMEDYREPACK INC.8e176ff2-ed3a-4909-94e1-6b9a3581a6212026-07-06Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
PAROXETINEPAROXETINE HYDROCHLORIDEREMEDYREPACK INC.beb87e2e-0a8f-43b6-b148-57f0b71915482026-07-02Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
PAROXETINEPAROXETINE HYDROCHLORIDEGolden State Medical Supply, Inc.e63fe922-b35a-406c-8737-f3f5e6d5a30d2026-05-27Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
PAROXETINEPAROXETINE HYDROCHLORIDEAphena Pharma Solutions - Tennessee, LLC4d3b4536-7900-223c-e063-6294a90a3d602026-03-17Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
PAROXETINEPAROXETINE HYDROCHLORIDEREMEDYREPACK INC.98d4f767-06e3-4d9b-b1ad-4b31f7e361302026-02-17Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
PAROXETINEPAROXETINE HYDROCHLORIDECardinal Health 107, LLC333dfd07-61f0-4b86-b4b5-b04adf64e49f2025-08-18Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
PAROXETINEPAROXETINE HYDROCHLORIDEMajor Pharmaceuticals84b1b1f0-d375-4fda-99af-9487f8ef50c72025-08-07Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
PAROXETINEPAROXETINE HYDROCHLORIDEApotex Corp.08320ea3-8f93-6f04-5d1c-f69af3eb5a812025-07-24Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
ndc (package): 60505-0084-9
ndc (product): 60505-0084
ndc11 (package): 60505008409
PAROXETINEPAROXETINE HYDROCHLORIDEAphena Pharma Solutions - Tennessee, LLC1801246b-02c3-430f-932a-b18cb0d13d1d2018-11-05Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356
PAROXETINEPAROXETINE HYDROCHLORIDEAphena Pharma Solutions - Tennessee, LLCa7128be7-7023-40c4-aa64-29d52145ae312018-10-17Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 075356
application number: ANDA075356

Additional Listing Data#

Finished product
Yes
Brand name base
PAROXETINE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PAROXETINE HYDROCHLORIDE ANHYDROUS30 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3I3T11UD2SInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1738483Internal RxNorm lookup
1738495Internal RxNorm lookup
1738503Internal RxNorm lookup
1738511Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
08320ea3-8f93-6f04-5d1c-f69af3eb5a81Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2ace441e-5ed1-9a56-64e5-302d887093bdProduct name720250107
ba9fc237-0e76-4ac8-d3c5-cdb4df9e9f7fProduct name420220524
200c61bf-0879-1df7-72b7-b72a8497b114Product name320171006
b430fc19-562d-420b-53a2-64d42b938631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60505-0084-1PAROXETINE30 in 1 BOTTLETABLET, FILM COATED3025
60505-0084-2PAROXETINE100 in 1 BOTTLETABLET, FILM COATED10025
60505-0084-4PAROXETINE1000 in 1 BOTTLETABLET, FILM COATED100025
60505-0084-5PAROXETINE10 in 1 BLISTER PACKTABLET, FILM COATED1025
60505-0084-5PAROXETINE10 in 1 CARTONTABLET, FILM COATED1025
60505-0084-9PAROXETINE90 in 1 BOTTLETABLET, FILM COATED9025

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60505-0084-1EA - Each60505-008459db11de-be77-4ee6-824c-bee7a731908d12012-07-24
60505-0084-2EA - Each60505-0084fa059b40-4016-416f-ae3f-8c908078b66612012-07-24
60505-0084-4EA - Each60505-0084e797d8aa-cb58-446d-a66a-41073b54f06112012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PAROXETINE HYDROCHLORIDE ANHYDROUSACTIVE INGREDIENT3I3T11UD2SPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
PAROXETINEACTIVE MOIETY41VRH5220HPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
HYDROXYPROPYL CELLULOSE (TYPE H)INACTIVE INGREDIENTRFW2ET671PPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1APAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]11
PAROXETINE HYDROCHLORIDE ANHYDROUSACTIVE INGREDIENT3I3T11UD2SPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
PAROXETINEACTIVE MOIETY41VRH5220HPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
HYDROXYPROPYL CELLULOSEINACTIVE INGREDIENTRFW2ET671PPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1APAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]5
PAROXETINE HYDROCHLORIDE ANHYDROUSACTIVE INGREDIENT3I3T11UD2SPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
PAROXETINEACTIVE MOIETY41VRH5220HPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
HYDROXYPROPYL CELLULOSE (TYPE H)INACTIVE INGREDIENTRFW2ET671PPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1APAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]4
PAROXETINE HYDROCHLORIDEACTIVE INGREDIENT3I3T11UD2SPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
PAROXETINE HYDROCHLORIDE ANHYDROUSACTIVE INGREDIENT3I3T11UD2SPAROXETINE TABLET, FILM COATED [DIRECTRX]1
PAROXETINEACTIVE MOIETY41VRH5220HPAROXETINE TABLET, FILM COATED [DIRECTRX]1
PAROXETINEACTIVE MOIETY41VRH5220HPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKPAROXETINE TABLET, FILM COATED [DIRECTRX]1
HYDROXYPROPYL CELLULOSEINACTIVE INGREDIENTRFW2ET671PPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
HYDROXYPROPYL CELLULOSE (TYPE H)INACTIVE INGREDIENTRFW2ET671PPAROXETINE TABLET, FILM COATED [DIRECTRX]1
HYPROMELLOSEINACTIVE INGREDIENT3NXW29V3WOPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOPAROXETINE TABLET, FILM COATED [DIRECTRX]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PAROXETINE TABLET, FILM COATED [DIRECTRX]1
POLYETHYLENE GLYCOLINACTIVE INGREDIENT3WJQ0SDW1APAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1APAROXETINE TABLET, FILM COATED [DIRECTRX]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2PAROXETINE TABLET, FILM COATED [DIRECTRX]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPPAROXETINE TABLET, FILM COATED [DIRECTRX]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60505-0084PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [APOTEX CORP.]24Current NDC, Legacy NDC, 6 package rows20250411_08320ea3-8f93-6f04-5d1c-f69af3eb5a81.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1738483PARoxetine HCl 10 MG Oral TabletPSN08320ea3-8f93-6f04-5d1c-f69af3eb5a8125
1738495PARoxetine HCl 20 MG Oral TabletPSN08320ea3-8f93-6f04-5d1c-f69af3eb5a8125
1738503PARoxetine HCl 30 MG Oral TabletPSN08320ea3-8f93-6f04-5d1c-f69af3eb5a8125
1738511PARoxetine HCl 40 MG Oral TabletPSN08320ea3-8f93-6f04-5d1c-f69af3eb5a8125
1738483paroxetine hydrochloride 10 MG Oral TabletSCD08320ea3-8f93-6f04-5d1c-f69af3eb5a8125
1738495paroxetine hydrochloride 20 MG Oral TabletSCD08320ea3-8f93-6f04-5d1c-f69af3eb5a8125
1738503paroxetine hydrochloride 30 MG Oral TabletSCD08320ea3-8f93-6f04-5d1c-f69af3eb5a8125
1738511paroxetine hydrochloride 40 MG Oral TabletSCD08320ea3-8f93-6f04-5d1c-f69af3eb5a8125
1738483PARoxetine HCl 10 MG Oral TabletPSN84b1b1f0-d375-4fda-99af-9487f8ef50c719
1738495PARoxetine HCl 20 MG Oral TabletPSN84b1b1f0-d375-4fda-99af-9487f8ef50c719
1738503PARoxetine HCl 30 MG Oral TabletPSN84b1b1f0-d375-4fda-99af-9487f8ef50c719
1738511PARoxetine HCl 40 MG Oral TabletPSN84b1b1f0-d375-4fda-99af-9487f8ef50c719
1738483paroxetine hydrochloride 10 MG Oral TabletSCD84b1b1f0-d375-4fda-99af-9487f8ef50c719
1738495paroxetine hydrochloride 20 MG Oral TabletSCD84b1b1f0-d375-4fda-99af-9487f8ef50c719
1738503paroxetine hydrochloride 30 MG Oral TabletSCD84b1b1f0-d375-4fda-99af-9487f8ef50c719
1738511paroxetine hydrochloride 40 MG Oral TabletSCD84b1b1f0-d375-4fda-99af-9487f8ef50c719
1738503PARoxetine HCl 30 MG Oral TabletPSN8e176ff2-ed3a-4909-94e1-6b9a3581a62118
1738503paroxetine hydrochloride 30 MG Oral TabletSCD8e176ff2-ed3a-4909-94e1-6b9a3581a62118
1738483PARoxetine HCl 10 MG Oral TabletPSNe63fe922-b35a-406c-8737-f3f5e6d5a30d17
1738495PARoxetine HCl 20 MG Oral TabletPSNe63fe922-b35a-406c-8737-f3f5e6d5a30d17
1738503PARoxetine HCl 30 MG Oral TabletPSNe63fe922-b35a-406c-8737-f3f5e6d5a30d17
1738511PARoxetine HCl 40 MG Oral TabletPSNe63fe922-b35a-406c-8737-f3f5e6d5a30d17
1738483paroxetine hydrochloride 10 MG Oral TabletSCDe63fe922-b35a-406c-8737-f3f5e6d5a30d17
1738495paroxetine hydrochloride 20 MG Oral TabletSCDe63fe922-b35a-406c-8737-f3f5e6d5a30d17
1738503paroxetine hydrochloride 30 MG Oral TabletSCDe63fe922-b35a-406c-8737-f3f5e6d5a30d17
1738511paroxetine hydrochloride 40 MG Oral TabletSCDe63fe922-b35a-406c-8737-f3f5e6d5a30d17
1738483PARoxetine HCl 10 MG Oral TabletPSNa93796a3-56fc-4af6-99ba-f76707c32e5d5
1738495PARoxetine HCl 20 MG Oral TabletPSNa93796a3-56fc-4af6-99ba-f76707c32e5d5
1738511PARoxetine HCl 40 MG Oral TabletPSNa93796a3-56fc-4af6-99ba-f76707c32e5d5
1738483paroxetine hydrochloride 10 MG Oral TabletSCDa93796a3-56fc-4af6-99ba-f76707c32e5d5
1738495paroxetine hydrochloride 20 MG Oral TabletSCDa93796a3-56fc-4af6-99ba-f76707c32e5d5
1738511paroxetine hydrochloride 40 MG Oral TabletSCDa93796a3-56fc-4af6-99ba-f76707c32e5d5
1738503PARoxetine HCl 30 MG Oral TabletPSN79b0eb99-95f8-4db4-ba30-503f32538ab83
1738503paroxetine hydrochloride 30 MG Oral TabletSCD79b0eb99-95f8-4db4-ba30-503f32538ab83
1738483PARoxetine HCl 10 MG Oral TabletPSNc9b57101-2455-463d-b8d7-b2316cecd67a1
1738495PARoxetine HCl 20 MG Oral TabletPSNc9b57101-2455-463d-b8d7-b2316cecd67a1
1738503PARoxetine HCl 30 MG Oral TabletPSNc9b57101-2455-463d-b8d7-b2316cecd67a1
1738511PARoxetine HCl 40 MG Oral TabletPSNc9b57101-2455-463d-b8d7-b2316cecd67a1
1738483paroxetine hydrochloride 10 MG Oral TabletSCDc9b57101-2455-463d-b8d7-b2316cecd67a1
1738495paroxetine hydrochloride 20 MG Oral TabletSCDc9b57101-2455-463d-b8d7-b2316cecd67a1
1738503paroxetine hydrochloride 30 MG Oral TabletSCDc9b57101-2455-463d-b8d7-b2316cecd67a1
1738511paroxetine hydrochloride 40 MG Oral TabletSCDc9b57101-2455-463d-b8d7-b2316cecd67a1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
60505-0084-96050500840990 TABLET, FILM COATED in 1 BOTTLE (60505-0084-9) 2003-09-080000-00-00NoNoCurrent