Package 71335-1964-2

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 71335-1964-2
Digits Only 7133519642
Product NDC 71335-1964
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-2)

Marketing

Marketing Status
Marketed Since 2021-02-10
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": "b4aff1e4-f7f7-4929-92fd-6c27babc38f5", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["9a8cb289-0332-4835-960f-32d273092d15"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-1)", "package_ndc": "71335-1964-1", "marketing_start_date": "20210210"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-2)", "package_ndc": "71335-1964-2", "marketing_start_date": "20210210"}, {"sample": false, "description": "28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-3)", "package_ndc": "71335-1964-3", "marketing_start_date": "20210210"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-4)", "package_ndc": "71335-1964-4", "marketing_start_date": "20210210"}], "brand_name": "DULOXETINE", "product_id": "71335-1964_b4aff1e4-f7f7-4929-92fd-6c27babc38f5", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-1964", "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": "ANDA206653", "marketing_category": "ANDA", "marketing_start_date": "20160120", "listing_expiration_date": "20261231"}