Package 70069-044-01
Brand: clonidine hydrochloride
Generic: clonidine hydrochloridePackage Facts
Identity
Package NDC
70069-044-01
Digits Only
7006904401
Product NDC
70069-044
Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01)
Marketing
Marketing Status
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": "b1e7ffe5-7d5f-4e02-a9c9-3d9ad3fac23e", "openfda": {"upc": ["0370069044018"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["1b4fb182-8194-4fdd-bf9b-f7e60e734179"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01)", "package_ndc": "70069-044-01", "marketing_start_date": "20250304"}], "brand_name": "Clonidine Hydrochloride", "product_id": "70069-044_b1e7ffe5-7d5f-4e02-a9c9-3d9ad3fac23e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70069-044", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA211433", "marketing_category": "ANDA", "marketing_start_date": "20250304", "listing_expiration_date": "20261231"}