Package 71335-2624-1

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 71335-2624-1
Digits Only 7133526241
Product NDC 71335-2624
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-1)

Marketing

Marketing Status
Marketed Since 2025-06-02
Brand duloxetine
Generic duloxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f8e683e1-9c7d-4ec2-bb01-6a3343f5f018", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["be0261c7-fb5e-4ba6-b7fb-13a1fecb5f75"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-1)", "package_ndc": "71335-2624-1", "marketing_start_date": "20250602"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-2)", "package_ndc": "71335-2624-2", "marketing_start_date": "20250602"}, {"sample": false, "description": "28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-3)", "package_ndc": "71335-2624-3", "marketing_start_date": "20250602"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-4)", "package_ndc": "71335-2624-4", "marketing_start_date": "20250602"}], "brand_name": "Duloxetine", "product_id": "71335-2624_f8e683e1-9c7d-4ec2-bb01-6a3343f5f018", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-2624", "generic_name": "Duloxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}