Package 50090-7812-1
Brand: duloxetine
Generic: duloxetinePackage Facts
Identity
Package NDC
50090-7812-1
Digits Only
5009078121
Product NDC
50090-7812
Description
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7812-1)
Marketing
Marketing Status
Brand
duloxetine
Generic
duloxetine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "22329868-1b97-471b-b501-453b9896cc28", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["7685a825-3c06-433d-ba98-4019c6ed2583"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7812-0)", "package_ndc": "50090-7812-0", "marketing_start_date": "20251208"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7812-1)", "package_ndc": "50090-7812-1", "marketing_start_date": "20251208"}], "brand_name": "Duloxetine", "product_id": "50090-7812_22329868-1b97-471b-b501-453b9896cc28", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-7812", "generic_name": "Duloxetine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20261231"}