Package 0093-3542-56

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 0093-3542-56
Digits Only 0093354256
Product NDC 0093-3542
Product ID 0093-3542_6b86d06c-1e99-484b-9643-5ed88511f045
Description

30 CAPSULE in 1 BOTTLE (0093-3542-56)

Marketing

Marketing Status
Marketed Since 2017-05-30
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": "6b86d06c-1e99-484b-9643-5ed88511f045", "openfda": {"upc": ["0300933546560", "0300933542562", "0300933543569", "0300933548564", "0300933545563", "0300933547567", "0300933544566"], "unii": ["57WVB6I2W0"], "rxcui": ["349591", "349592", "349593", "349594", "349595", "608139", "608143"], "spl_set_id": ["4953df7b-ccdb-452c-8699-5fd7259609b4"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (0093-3542-56)", "package_ndc": "0093-3542-56", "marketing_start_date": "20170530"}], "brand_name": "Atomoxetine", "product_id": "0093-3542_6b86d06c-1e99-484b-9643-5ed88511f045", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "0093-3542", "generic_name": "Atomoxetine", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA079022", "marketing_category": "ANDA", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}