Package 49252-008-11

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 49252-008-11
Digits Only 4925200811
Product NDC 49252-008
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-11)

Marketing

Marketing Status
Marketed Since 2015-12-05
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": "3fb45d3e-3fbc-8814-e063-6294a90a4a70", "openfda": {"upc": ["0349252007574", "0349252009103", "0349252008106", "0349252008571", "0349252009578"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["eab90059-ea1c-46c1-884d-c15e7c562a01"], "manufacturer_name": ["Inventia Healthcare Limited."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-10)", "package_ndc": "49252-008-10", "marketing_start_date": "20151205"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-11)", "package_ndc": "49252-008-11", "marketing_start_date": "20151205"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-12)", "package_ndc": "49252-008-12", "marketing_start_date": "20151205"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-18)", "package_ndc": "49252-008-18", "marketing_start_date": "20151205"}, {"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (49252-008-57)", "package_ndc": "49252-008-57", "marketing_start_date": "20151205"}], "brand_name": "duloxetine", "product_id": "49252-008_3fb45d3e-3fbc-8814-e063-6294a90a4a70", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "49252-008", "generic_name": "duloxetine", "labeler_name": "Inventia Healthcare Limited.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA202336", "marketing_category": "ANDA", "marketing_start_date": "20151205", "listing_expiration_date": "20261231"}