Package 68180-295-09

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 68180-295-09
Digits Only 6818029509
Product NDC 68180-295
Product ID 68180-295_7efa28f3-0b15-4e1c-835f-2f1dff37bee8
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-09)

Marketing

Marketing Status
Marketed Since 2013-12-11
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": "7efa28f3-0b15-4e1c-835f-2f1dff37bee8", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934", "616402"], "spl_set_id": ["829a4f51-c882-4b64-81f3-abfb03a52ebe"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-03)", "package_ndc": "68180-295-03", "marketing_start_date": "20140306"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-06)", "package_ndc": "68180-295-06", "marketing_start_date": "20131211"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-09)", "package_ndc": "68180-295-09", "marketing_start_date": "20131211"}], "brand_name": "Duloxetine", "product_id": "68180-295_7efa28f3-0b15-4e1c-835f-2f1dff37bee8", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68180-295", "generic_name": "Duloxetine", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}