Package 60429-164-60

Brand: duloxetine delayed-release

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60429-164-60
Digits Only 6042916460
Product NDC 60429-164
Description

60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-164-60)

Marketing

Marketing Status
Marketed Since 2014-06-11
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": "3a8cefd0-9db7-8cd0-e063-6394a90a5996", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["f535fcd2-a50a-4423-85d9-705fd2d9a470"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-164-60)", "package_ndc": "60429-164-60", "marketing_start_date": "20140611"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "60429-164_3a8cefd0-9db7-8cd0-e063-6394a90a5996", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60429-164", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}