Package 63187-612-90

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-612-90
Digits Only 6318761290
Product NDC 63187-612
Product ID 63187-612_9e0aea8e-e493-432d-a390-5f6d7944ba69
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-90)

Marketing

Marketing Status
Marketed Since 2018-12-01
Brand duloxetine
Generic duloxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Duloxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9e0aea8e-e493-432d-a390-5f6d7944ba69", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["c34f6115-f447-450f-8c83-58f3c51a76c9"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-30)", "package_ndc": "63187-612-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-60)", "package_ndc": "63187-612-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-90)", "package_ndc": "63187-612-90", "marketing_start_date": "20181201"}], "brand_name": "Duloxetine", "product_id": "63187-612_9e0aea8e-e493-432d-a390-5f6d7944ba69", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63187-612", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090778", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}