Package 63187-735-60

Brand: duloxetine delayed-release

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-735-60
Digits Only 6318773560
Product NDC 63187-735
Description

60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-60)

Marketing

Marketing Status
Marketed Since 2016-07-01
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": "c40e425f-a9b7-4ab5-93ea-6e14ae0b77f9", "openfda": {"upc": ["0363187735302"], "unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["22a8cc15-17fb-4c4e-8d2a-de5755ed6031"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-30)", "package_ndc": "63187-735-30", "marketing_start_date": "20160701"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-60)", "package_ndc": "63187-735-60", "marketing_start_date": "20160701"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-90)", "package_ndc": "63187-735-90", "marketing_start_date": "20160701"}], "brand_name": "DULOXETINE DELAYED-RELEASE", "product_id": "63187-735_c40e425f-a9b7-4ab5-93ea-6e14ae0b77f9", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63187-735", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DULOXETINE", "brand_name_suffix": "DELAYED-RELEASE", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}