Package 70518-4337-0

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 70518-4337-0
Digits Only 7051843370
Product NDC 70518-4337
Product ID 70518-4337_4030d12b-a63d-6c7e-e063-6394a90a7941
Description

30 POUCH in 1 BOX (70518-4337-0) / 1 CAPSULE in 1 POUCH (70518-4337-1)

Marketing

Marketing Status
Marketed Since 2025-05-12
Brand atomoxetine
Generic atomoxetine
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4030d12b-a63d-6c7e-e063-6394a90a7941", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["608139"], "spl_set_id": ["d7002d75-edad-4141-91bf-7eebf50ad1aa"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-4337-0)  / 1 CAPSULE in 1 POUCH (70518-4337-1)", "package_ndc": "70518-4337-0", "marketing_start_date": "20250512"}], "brand_name": "Atomoxetine", "product_id": "70518-4337_4030d12b-a63d-6c7e-e063-6394a90a7941", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "70518-4337", "generic_name": "Atomoxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA090609", "marketing_category": "ANDA", "marketing_start_date": "20250512", "listing_expiration_date": "20261231"}