Package 50090-6863-0

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6863-0
Digits Only 5009068630
Product NDC 50090-6863
Product ID 50090-6863_da9f6f45-acd7-4a27-a847-436610344cf0
Description

90 CAPSULE in 1 BOTTLE (50090-6863-0)

Marketing

Marketing Status
Marketed Since 2023-12-04
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "da9f6f45-acd7-4a27-a847-436610344cf0", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["08f3c11c-9ba0-4c53-bf31-264725e611ea"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-6863-0)", "package_ndc": "50090-6863-0", "marketing_start_date": "20231204"}], "brand_name": "Fluoxetine", "product_id": "50090-6863_da9f6f45-acd7-4a27-a847-436610344cf0", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6863", "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"}