Package 72162-1495-1

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1495-1
Digits Only 7216214951
Product NDC 72162-1495
Description

100 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1495-1)

Marketing

Marketing Status
Marketed Since 2023-04-20
Brand fluoxetine hydrochloride
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "69fb683e-2ff5-4a53-af97-b5b87f8dfa94", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["248642"], "spl_set_id": ["a04a5bed-d051-4bb4-ae20-b09b10d5c181"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1495-1)", "package_ndc": "72162-1495-1", "marketing_start_date": "20230420"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1495-3)", "package_ndc": "72162-1495-3", "marketing_start_date": "20230420"}], "brand_name": "fluoxetine hydrochloride", "product_id": "72162-1495_69fb683e-2ff5-4a53-af97-b5b87f8dfa94", "dosage_form": "TABLET, COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-1495", "generic_name": "fluoxetine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluoxetine hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203836", "marketing_category": "ANDA", "marketing_start_date": "20160822", "listing_expiration_date": "20261231"}