paroxetine

Generic: paroxetine hydrochloride

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name paroxetine
Generic Name paroxetine hydrochloride
Labeler golden state medical supply, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

paroxetine hydrochloride anhydrous 40 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 60429-737
Product ID 60429-737_43d3982d-7dba-7704-e063-6394a90a9988
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075356
Listing Expiration 2026-12-31
Marketing Start 2003-07-30

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60429737
Hyphenated Format 60429-737

Supplemental Identifiers

RxCUI
1738483 1738495 1738503 1738511
UNII
3I3T11UD2S

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name paroxetine (source: ndc)
Generic Name paroxetine hydrochloride (source: ndc)
Application Number ANDA075356 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (60429-737-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (60429-737-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (60429-737-90)
source: ndc

Packages (3)

60429-737-10 1000 TABLET, FILM COATED in 1 BOTTLE (60429-737-10) 60429-737-30 30 TABLET, FILM COATED in 1 BOTTLE (60429-737-30) 60429-737-90 90 TABLET, FILM COATED in 1 BOTTLE (60429-737-90)

Ingredients (1)

paroxetine hydrochloride anhydrous (40 mg/1)

Linked Drug Pages (1)

PAROXETINE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43d3982d-7dba-7704-e063-6394a90a9988", "openfda": {"unii": ["3I3T11UD2S"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["e63fe922-b35a-406c-8737-f3f5e6d5a30d"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60429-737-10)", "package_ndc": "60429-737-10", "marketing_start_date": "20190101"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60429-737-30)", "package_ndc": "60429-737-30", "marketing_start_date": "20190101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (60429-737-90)", "package_ndc": "60429-737-90", "marketing_start_date": "20190101"}], "brand_name": "PAROXETINE", "product_id": "60429-737_43d3982d-7dba-7704-e063-6394a90a9988", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60429-737", "generic_name": "paroxetine hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE ANHYDROUS", "strength": "40 mg/1"}], "application_number": "ANDA075356", "marketing_category": "ANDA", "marketing_start_date": "20030730", "listing_expiration_date": "20261231"}