Package 72162-2542-3

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 72162-2542-3
Digits Only 7216225423
Product NDC 72162-2542
Description

30 CAPSULE in 1 BOTTLE (72162-2542-3)

Marketing

Marketing Status
Marketed Since 2025-10-16
Brand atomoxetine
Generic atomoxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cad2dce9-dde2-443e-b51b-dff519b277ba", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349592"], "spl_set_id": ["9c1f858c-8721-49e3-be8b-bf180e89ff42"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72162-2542-3)", "package_ndc": "72162-2542-3", "marketing_start_date": "20251016"}], "brand_name": "Atomoxetine", "product_id": "72162-2542_cad2dce9-dde2-443e-b51b-dff519b277ba", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "72162-2542", "generic_name": "Atomoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "18 mg/1"}], "application_number": "ANDA079021", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}