Package 63629-2063-1
Brand: duloxetine delayed-release
Generic: duloxetine hydrochloridePackage Facts
Identity
Package NDC
63629-2063-1
Digits Only
6362920631
Product NDC
63629-2063
Description
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-2063-1)
Marketing
Marketing Status
Brand
duloxetine delayed-release
Generic
duloxetine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d9d5d315-85a9-4ff9-b185-06c06e16ec00", "openfda": {"unii": ["9044SC542W"], "rxcui": ["616402"], "spl_set_id": ["675f999d-46b2-45da-b17e-58cc2ba180b1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-2063-1)", "package_ndc": "63629-2063-1", "marketing_start_date": "20180521"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "63629-2063_d9d5d315-85a9-4ff9-b185-06c06e16ec00", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63629-2063", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20180521", "listing_expiration_date": "20261231"}