Package 60760-759-30

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 60760-759-30
Digits Only 6076075930
Product NDC 60760-759
Product ID 60760-759_39fa5490-f66d-79af-e063-6294a90a22ea
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-759-30)

Marketing

Marketing Status
Marketed Since 2025-07-15
Brand duloxetine
Generic duloxetine
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": "39fa5490-f66d-79af-e063-6294a90a22ea", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["39fa4247-e864-f653-e063-6394a90ac98d"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-759-30)", "package_ndc": "60760-759-30", "marketing_start_date": "20250715"}], "brand_name": "Duloxetine", "product_id": "60760-759_39fa5490-f66d-79af-e063-6294a90a22ea", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-759", "generic_name": "Duloxetine", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20261231"}