Package 70247-012-06

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 70247-012-06
Digits Only 7024701206
Product NDC 70247-012
Product ID 70247-012_435c56f7-5995-3906-e063-6394a90af073
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-012-06)

Marketing

Marketing Status
Marketed Since 2018-05-08
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": "435c56f7-5995-3906-e063-6394a90af073", "openfda": {"upc": ["0370247013034", "0370247014031", "0370247014062", "0370247012068", "0370247014505", "0370247013096", "0370247013102"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["e428429e-e1ea-40e1-870f-134533dc3aa1"], "manufacturer_name": ["Qingdao BAHEAL Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-012-06)", "package_ndc": "70247-012-06", "marketing_start_date": "20180508"}], "brand_name": "duloxetine", "product_id": "70247-012_435c56f7-5995-3906-e063-6394a90af073", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70247-012", "generic_name": "Duloxetine", "labeler_name": "Qingdao BAHEAL Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA210599", "marketing_category": "ANDA", "marketing_start_date": "20180505", "listing_expiration_date": "20261231"}