Package 50090-6143-0

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 50090-6143-0
Digits Only 5009061430
Product NDC 50090-6143
Product ID 50090-6143_a726ffd7-e7bd-4005-8b8a-b4d9bb58b67f
Description

30 CAPSULE in 1 BOTTLE (50090-6143-0)

Marketing

Marketing Status
Marketed Since 2022-10-04
Brand atomoxetine
Generic atomoxetine
Sample Package No

Linked Drug Pages (1)

Atomoxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a726ffd7-e7bd-4005-8b8a-b4d9bb58b67f", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349594"], "spl_set_id": ["0782204e-56a3-4439-9fb8-194da9487049"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-6143-0)", "package_ndc": "50090-6143-0", "marketing_start_date": "20221004"}], "brand_name": "Atomoxetine", "product_id": "50090-6143_a726ffd7-e7bd-4005-8b8a-b4d9bb58b67f", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-6143", "generic_name": "Atomoxetine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA202682", "marketing_category": "ANDA", "marketing_start_date": "20210311", "listing_expiration_date": "20261231"}