Package 70518-4313-0

Brand: atomoxetine hydrochloride

Generic: atomoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4313-0
Digits Only 7051843130
Product NDC 70518-4313
Product ID 70518-4313_402dde79-775f-0a84-e063-6294a90a60c0
Description

30 POUCH in 1 BOX (70518-4313-0) / 1 CAPSULE in 1 POUCH (70518-4313-1)

Marketing

Marketing Status
Marketed Since 2025-03-19
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": "402dde79-775f-0a84-e063-6294a90a60c0", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349591"], "spl_set_id": ["6d7ea8f7-981c-4acc-aeaf-7516325bfc0c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-4313-0)  / 1 CAPSULE in 1 POUCH (70518-4313-1)", "package_ndc": "70518-4313-0", "marketing_start_date": "20250319"}], "brand_name": "Atomoxetine Hydrochloride", "product_id": "70518-4313_402dde79-775f-0a84-e063-6294a90a60c0", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "70518-4313", "generic_name": "atomoxetine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine Hydrochloride", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078983", "marketing_category": "ANDA", "marketing_start_date": "20250319", "listing_expiration_date": "20261231"}