Package 60687-734-01

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-734-01
Digits Only 6068773401
Product NDC 60687-734
Product ID 60687-734_3140ed8f-e974-d45b-e063-6294a90a725d
Description

100 BLISTER PACK in 1 CARTON (60687-734-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-734-11)

Marketing

Marketing Status
Discontinued 2026-03-31
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": "3140ed8f-e974-d45b-e063-6294a90a725d", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["7da3d2c4-8793-4da3-b54a-ae20717cf066"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-734-01)  / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-734-11)", "package_ndc": "60687-734-01", "marketing_end_date": "20260331", "marketing_start_date": "20230403"}], "brand_name": "Duloxetine", "product_id": "60687-734_3140ed8f-e974-d45b-e063-6294a90a725d", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60687-734", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "American Health Packaging", "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_end_date": "20260331", "marketing_start_date": "20230403"}