Package 0904-6908-04

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 0904-6908-04
Digits Only 0904690804
Product NDC 0904-6908
Product ID 0904-6908_e4c4122b-6772-46a0-aaaa-3815e6a9736f
Description

30 BLISTER PACK in 1 CARTON (0904-6908-04) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-02-23
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": "e4c4122b-6772-46a0-aaaa-3815e6a9736f", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349594"], "spl_set_id": ["f98c3424-1c43-43e4-8bca-2e3430f50c63"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6908-04)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6908-04", "marketing_start_date": "20180223"}], "brand_name": "Atomoxetine", "product_id": "0904-6908_e4c4122b-6772-46a0-aaaa-3815e6a9736f", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "0904-6908", "generic_name": "Atomoxetine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA090609", "marketing_category": "ANDA", "marketing_start_date": "20180223", "listing_expiration_date": "20261231"}