Package 71335-0509-2

Brand: duloxetine delayed-release

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0509-2
Digits Only 7133505092
Product NDC 71335-0509
Description

28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-2)

Marketing

Marketing Status
Marketed Since 2024-05-29
Brand duloxetine delayed-release
Generic duloxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f56840bd-a85a-489d-ae5a-cf6fe696f1a8", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["0c82422a-d493-4dda-8626-0d9baa25db8c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-1)", "package_ndc": "71335-0509-1", "marketing_start_date": "20210224"}, {"sample": false, "description": "28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-2)", "package_ndc": "71335-0509-2", "marketing_start_date": "20240529"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-3)", "package_ndc": "71335-0509-3", "marketing_start_date": "20210224"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-4)", "package_ndc": "71335-0509-4", "marketing_start_date": "20210407"}, {"sample": false, "description": "180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-5)", "package_ndc": "71335-0509-5", "marketing_start_date": "20220831"}, {"sample": false, "description": "120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-6)", "package_ndc": "71335-0509-6", "marketing_start_date": "20240529"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "71335-0509_f56840bd-a85a-489d-ae5a-cf6fe696f1a8", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-0509", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}