Package 71034-001-60

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71034-001-60
Digits Only 7103400160
Product NDC 71034-001
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-001-60)

Marketing

Marketing Status
Marketed Since 2017-12-01
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": "b2b1f979-6a18-ad41-e053-2995a90ad14a", "openfda": {"upc": ["0371034001609"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["7676af27-4d8f-49c4-a50f-6b0892e73c8f"], "manufacturer_name": ["Xiamen LP Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-001-60)", "package_ndc": "71034-001-60", "marketing_start_date": "20171201"}], "brand_name": "Clonidine Hydrochloride", "product_id": "71034-001_b2b1f979-6a18-ad41-e053-2995a90ad14a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "71034-001", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Xiamen LP Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA209757", "marketing_category": "ANDA", "marketing_start_date": "20171201", "listing_expiration_date": "20261231"}