Package 71335-2361-2

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 71335-2361-2
Digits Only 7133523612
Product NDC 71335-2361
Description

60 CAPSULE in 1 BOTTLE (71335-2361-2)

Marketing

Marketing Status
Marketed Since 2024-05-28
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": "e99189a3-22df-4bc2-85b2-1641fba9ed01", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349595"], "spl_set_id": ["97a4aa63-0877-40e5-94c4-ea487db5691d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-2361-1)", "package_ndc": "71335-2361-1", "marketing_start_date": "20240528"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-2361-2)", "package_ndc": "71335-2361-2", "marketing_start_date": "20240528"}], "brand_name": "atomoxetine", "product_id": "71335-2361_e99189a3-22df-4bc2-85b2-1641fba9ed01", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71335-2361", "generic_name": "atomoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA079019", "marketing_category": "ANDA", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}