Package 50090-7784-0

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 50090-7784-0
Digits Only 5009077840
Product NDC 50090-7784
Product ID 50090-7784_ff8516a1-b0de-4bd3-9945-523089b42128
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7784-0)

Marketing

Marketing Status
Marketed Since 2025-11-21
Brand duloxetine
Generic duloxetine
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": "ff8516a1-b0de-4bd3-9945-523089b42128", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["e0381ead-d8bc-43fa-9f12-e0fefcaf7f3d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7784-0)", "package_ndc": "50090-7784-0", "marketing_start_date": "20251121"}], "brand_name": "Duloxetine", "product_id": "50090-7784_ff8516a1-b0de-4bd3-9945-523089b42128", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-7784", "generic_name": "Duloxetine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}