Package 70518-3295-0

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3295-0
Digits Only 7051832950
Product NDC 70518-3295
Description

30 TABLET in 1 BLISTER PACK (70518-3295-0)

Marketing

Marketing Status
Marketed Since 2021-12-14
Brand clonidine hydrochloride
Generic clonidine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38dd1489-8625-2e37-e063-6394a90a00ee", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884185"], "spl_set_id": ["e413efdf-980b-4b33-80f1-5be899a10f01"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3295-0)", "package_ndc": "70518-3295-0", "marketing_start_date": "20211214"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-3295-1)", "package_ndc": "70518-3295-1", "marketing_start_date": "20250630"}], "brand_name": "Clonidine Hydrochloride", "product_id": "70518-3295_38dd1489-8625-2e37-e063-6394a90a00ee", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-3295", "generic_name": "Clonidine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA202297", "marketing_category": "ANDA", "marketing_start_date": "20211214", "listing_expiration_date": "20261231"}