Package 0615-8263-39

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8263-39
Digits Only 0615826339
Product NDC 0615-8263
Description

30 CAPSULE in 1 BLISTER PACK (0615-8263-39)

Marketing

Marketing Status
Marketed Since 2019-01-10
Brand amantadine hydrochloride
Generic amantadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "056d9ef2-8e38-40eb-8d3a-0d753e018030", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["b54064bc-b3e1-4d83-be40-fcaddd2e99d0"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (0615-8263-39)", "package_ndc": "0615-8263-39", "marketing_start_date": "20190110"}], "brand_name": "Amantadine Hydrochloride", "product_id": "0615-8263_056d9ef2-8e38-40eb-8d3a-0d753e018030", "dosage_form": "CAPSULE", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "0615-8263", "generic_name": "Amantadine Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine Hydrochloride", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA209171", "marketing_category": "ANDA", "marketing_start_date": "20170101", "listing_expiration_date": "20261231"}