Package 71610-402-60

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-402-60
Digits Only 7161040260
Product NDC 71610-402
Product ID 71610-402_157fe8e5-a477-47eb-adac-6b9ffe571af9
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-402-60)

Marketing

Marketing Status
Marketed Since 2020-02-26
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": "157fe8e5-a477-47eb-adac-6b9ffe571af9", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930"], "spl_set_id": ["b102b8e6-d58f-419c-bb35-720bafa13294"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-402-60)", "package_ndc": "71610-402-60", "marketing_start_date": "20200226"}], "brand_name": "Duloxetine", "product_id": "71610-402_157fe8e5-a477-47eb-adac-6b9ffe571af9", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71610-402", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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"}