Package 71335-2162-1

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 71335-2162-1
Digits Only 7133521621
Product NDC 71335-2162
Product ID 71335-2162_3767a887-2273-a522-e063-6394a90a3fbc
Description

30 CAPSULE in 1 BOTTLE (71335-2162-1)

Marketing

Marketing Status
Marketed Since 2022-09-07
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": "3767a887-2273-a522-e063-6394a90a3fbc", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349594"], "spl_set_id": ["d4fe9217-1853-4f8b-9a93-77e511554ca1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-2162-1)", "package_ndc": "71335-2162-1", "marketing_start_date": "20220907"}], "brand_name": "Atomoxetine", "product_id": "71335-2162_3767a887-2273-a522-e063-6394a90a3fbc", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71335-2162", "generic_name": "Atomoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA079016", "marketing_category": "ANDA", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}