Package 50090-7232-0

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7232-0
Digits Only 5009072320
Product NDC 50090-7232
Description

90 CAPSULE in 1 BOTTLE (50090-7232-0)

Marketing

Marketing Status
Marketed Since 2024-08-26
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "19fd63e7-d4bf-46c7-b13e-9cab103447b9", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["2f302db0-1c88-44cf-8258-3c1c60afb5a4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-7232-0)", "package_ndc": "50090-7232-0", "marketing_start_date": "20240826"}], "brand_name": "Fluoxetine", "product_id": "50090-7232_19fd63e7-d4bf-46c7-b13e-9cab103447b9", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7232", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20261231"}