Package 50090-6986-0

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6986-0
Digits Only 5009069860
Product NDC 50090-6986
Description

90 CAPSULE in 1 BOTTLE (50090-6986-0)

Marketing

Marketing Status
Marketed Since 2023-12-27
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f0ec020d-32d3-49cc-a35c-4ae91771a8ea", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["578ca8f8-86eb-4247-a0b3-50c3837a982e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-6986-0)", "package_ndc": "50090-6986-0", "marketing_start_date": "20231227"}], "brand_name": "Fluoxetine", "product_id": "50090-6986_f0ec020d-32d3-49cc-a35c-4ae91771a8ea", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6986", "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": "20 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20261231"}