Package 71335-9650-1
Brand: paroxetine hydrochloride
Generic: paroxetine hydrochloridePackage Facts
Identity
Package NDC
71335-9650-1
Digits Only
7133596501
Product NDC
71335-9650
Description
30 TABLET, FILM COATED in 1 BOTTLE (71335-9650-1)
Marketing
Marketing Status
Brand
paroxetine hydrochloride
Generic
paroxetine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "52e74299-f193-408d-9d0d-e48398a1734a", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738503"], "spl_set_id": ["c3c204df-6b7d-42fb-8794-4f38064ed963"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-9650-1)", "package_ndc": "71335-9650-1", "marketing_start_date": "20230328"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-9650-2)", "package_ndc": "71335-9650-2", "marketing_start_date": "20240906"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-9650-3)", "package_ndc": "71335-9650-3", "marketing_start_date": "20240906"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-9650-4)", "package_ndc": "71335-9650-4", "marketing_start_date": "20240906"}], "brand_name": "paroxetine hydrochloride", "product_id": "71335-9650_52e74299-f193-408d-9d0d-e48398a1734a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-9650", "generic_name": "paroxetine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "paroxetine hydrochloride", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "30 mg/1"}], "application_number": "ANDA076968", "marketing_category": "ANDA", "marketing_start_date": "20221114", "listing_expiration_date": "20261231"}