Package 68001-568-06

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68001-568-06
Digits Only 6800156806
Product NDC 68001-568
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-568-06)

Marketing

Marketing Status
Marketed Since 2023-08-24
Brand clonidine hydrochloride
Generic clonidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c4f16d2-af44-ddf6-e063-6294a90aae36", "openfda": {"upc": ["0368001568067"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["f34ae077-4ace-4e0a-bc87-d559b1c5bf2f"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-568-06)", "package_ndc": "68001-568-06", "marketing_start_date": "20230824"}], "brand_name": "Clonidine hydrochloride", "product_id": "68001-568_3c4f16d2-af44-ddf6-e063-6294a90aae36", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "68001-568", "generic_name": "Clonidine hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA209686", "marketing_category": "ANDA", "marketing_start_date": "20230824", "listing_expiration_date": "20261231"}