Package 71610-449-09

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-449-09
Digits Only 7161044909
Product NDC 71610-449
Product ID 71610-449_6e5cec35-31fa-4db7-a681-cd264ebd6cbf
Description

9000 TABLET in 1 BOTTLE (71610-449-09)

Marketing

Marketing Status
Marketed Since 2020-07-28
Brand clonidine hydrochloride
Generic clonidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Clonidine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6e5cec35-31fa-4db7-a681-cd264ebd6cbf", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["00d1562d-b4eb-4d89-95de-0aacee7a82a5"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 TABLET in 1 BOTTLE (71610-449-09)", "package_ndc": "71610-449-09", "marketing_start_date": "20200728"}], "brand_name": "Clonidine hydrochloride", "product_id": "71610-449_6e5cec35-31fa-4db7-a681-cd264ebd6cbf", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "71610-449", "generic_name": "Clonidine hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA070923", "marketing_category": "ANDA", "marketing_start_date": "20170601", "listing_expiration_date": "20261231"}