Package 50268-059-13

Brand: atomoxetine hydrochloride

Generic: atomoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-059-13
Digits Only 5026805913
Product NDC 50268-059
Product ID 50268-059_4587bd5f-1bd2-c809-e063-6294a90adf87
Description

30 BLISTER PACK in 1 BOX (50268-059-13) / 1 CAPSULE in 1 BLISTER PACK (50268-059-11)

Marketing

Marketing Status
Marketed Since 2020-07-07
Brand atomoxetine hydrochloride
Generic atomoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Atomoxetine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4587bd5f-1bd2-c809-e063-6294a90adf87", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349595"], "spl_set_id": ["a9df4617-b406-70ba-e053-2995a90a28e8"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX (50268-059-13)  / 1 CAPSULE in 1 BLISTER PACK (50268-059-11)", "package_ndc": "50268-059-13", "marketing_start_date": "20200707"}], "brand_name": "Atomoxetine Hydrochloride", "product_id": "50268-059_4587bd5f-1bd2-c809-e063-6294a90adf87", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50268-059", "generic_name": "atomoxetine hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine Hydrochloride", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA078983", "marketing_category": "ANDA", "marketing_start_date": "20200707", "listing_expiration_date": "20261231"}