Package 50268-057-13

Brand: atomoxetine hydrochloride

Generic: atomoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-057-13
Digits Only 5026805713
Product NDC 50268-057
Product ID 50268-057_47e225fb-3d2a-4f80-e063-6394a90aff85
Description

30 BLISTER PACK in 1 BOX (50268-057-13) / 1 CAPSULE in 1 BLISTER PACK (50268-057-11)

Marketing

Marketing Status
Marketed Since 2020-02-13
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": "47e225fb-3d2a-4f80-e063-6394a90aff85", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349593", "349594"], "spl_set_id": ["9e787cc2-5d0f-f231-e053-2a95a90ae99a"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX (50268-057-13)  / 1 CAPSULE in 1 BLISTER PACK (50268-057-11)", "package_ndc": "50268-057-13", "marketing_start_date": "20200213"}], "brand_name": "Atomoxetine Hydrochloride", "product_id": "50268-057_47e225fb-3d2a-4f80-e063-6394a90aff85", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50268-057", "generic_name": "atomoxetine hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine Hydrochloride", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA078983", "marketing_category": "ANDA", "marketing_start_date": "20200213", "listing_expiration_date": "20271231"}