Package 60760-951-60

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-951-60
Digits Only 6076095160
Product NDC 60760-951
Product ID 60760-951_0191629f-f9f4-6ad0-e063-6294a90a773f
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-951-60)

Marketing

Marketing Status
Marketed Since 2023-07-24
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": "0191629f-f9f4-6ad0-e063-6294a90a773f", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["019160f0-44fa-7e04-e063-6394a90a98e6"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-951-60)", "package_ndc": "60760-951-60", "marketing_start_date": "20230724"}], "brand_name": "Duloxetine", "product_id": "60760-951_0191629f-f9f4-6ad0-e063-6294a90a773f", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-951", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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"}