Package 60687-326-25

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 60687-326-25
Digits Only 6068732625
Product NDC 60687-326
Product ID 60687-326_2759be5a-a8a1-2119-e063-6394a90a38ac
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-326-25) / 1 CAPSULE in 1 BLISTER PACK (60687-326-95)

Marketing

Marketing Status
Marketed Since 2017-09-08
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": "2759be5a-a8a1-2119-e063-6394a90a38ac", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349593", "349594"], "spl_set_id": ["10d36b32-0202-4c03-8a1a-cd5d53f231e7"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-326-25)  / 1 CAPSULE in 1 BLISTER PACK (60687-326-95)", "package_ndc": "60687-326-25", "marketing_start_date": "20170908"}], "brand_name": "Atomoxetine", "product_id": "60687-326_2759be5a-a8a1-2119-e063-6394a90a38ac", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "60687-326", "generic_name": "Atomoxetine", "labeler_name": "American Health Packaging", "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": "20170908", "listing_expiration_date": "20261231"}