Package 71335-2625-1

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 71335-2625-1
Digits Only 7133526251
Product NDC 71335-2625
Product ID 71335-2625_6606e4e5-52f7-4c60-b6ac-f7f76d926c6e
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2625-1)

Marketing

Marketing Status
Marketed Since 2025-06-02
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": "6606e4e5-52f7-4c60-b6ac-f7f76d926c6e", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["5584c5ed-cab6-4c8b-8307-41e5d77704d0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2625-1)", "package_ndc": "71335-2625-1", "marketing_start_date": "20250602"}], "brand_name": "Duloxetine", "product_id": "71335-2625_6606e4e5-52f7-4c60-b6ac-f7f76d926c6e", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-2625", "generic_name": "Duloxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}