Package 63629-8748-1

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 63629-8748-1
Digits Only 6362987481
Product NDC 63629-8748
Description

30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-8748-1)

Marketing

Marketing Status
Marketed Since 2013-12-17
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": "b9f90234-c0e9-4c82-8787-d441d2181384", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["726b3c3e-8266-4a8a-a426-899cecd4f87e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-8748-1)", "package_ndc": "63629-8748-1", "marketing_start_date": "20131217"}], "brand_name": "Duloxetine", "product_id": "63629-8748_b9f90234-c0e9-4c82-8787-d441d2181384", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63629-8748", "generic_name": "Duloxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20131217", "listing_expiration_date": "20261231"}