Package 68788-9301-0

Brand: duloxetine delayed-release

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-9301-0
Digits Only 6878893010
Product NDC 68788-9301
Description

6 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-9301-0)

Marketing

Marketing Status
Marketed Since 2015-03-23
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": "7ad6ae66-a039-4738-beab-67dbfd83568d", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["49821f58-a5a6-47c5-96d1-f673ef2f4bd5"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-9301-0)", "package_ndc": "68788-9301-0", "marketing_start_date": "20150323"}, {"sample": false, "description": "10 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-9301-1)", "package_ndc": "68788-9301-1", "marketing_start_date": "20150323"}, {"sample": false, "description": "20 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-9301-2)", "package_ndc": "68788-9301-2", "marketing_start_date": "20150323"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-9301-3)", "package_ndc": "68788-9301-3", "marketing_start_date": "20150323"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-9301-6)", "package_ndc": "68788-9301-6", "marketing_start_date": "20150323"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-9301-9)", "package_ndc": "68788-9301-9", "marketing_start_date": "20150323"}], "brand_name": "DULOXETINE DELAYED-RELEASE", "product_id": "68788-9301_7ad6ae66-a039-4738-beab-67dbfd83568d", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-9301", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DULOXETINE", "brand_name_suffix": "DELAYED-RELEASE", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20150323", "listing_expiration_date": "20261231"}