Package 68071-2699-1

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2699-1
Digits Only 6807126991
Product NDC 68071-2699
Description

100 TABLET in 1 BOTTLE (68071-2699-1)

Marketing

Marketing Status
Marketed Since 2022-05-18
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": "30b5a4cf-2c74-1eee-e063-6394a90a2b59", "openfda": {"upc": ["0368071269918"], "unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["df4b087e-a81a-1321-e053-2995a90a2b9f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-2699-1)", "package_ndc": "68071-2699-1", "marketing_start_date": "20220518"}], "brand_name": "Clonidine Hydrochloride", "product_id": "68071-2699_30b5a4cf-2c74-1eee-e063-6394a90a2b59", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "68071-2699", "generic_name": "Clonidine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA070974", "marketing_category": "ANDA", "marketing_start_date": "19950103", "listing_expiration_date": "20261231"}