Package 71335-2889-1

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2889-1
Digits Only 7133528891
Product NDC 71335-2889
Description

500 TABLET in 1 BOTTLE (71335-2889-1)

Marketing

Marketing Status
Marketed Since 2025-10-29
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": "42540d3c-5254-6bc7-e063-6294a90adf98", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["60171b1d-03af-4849-a030-6260192b11ce"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-2889-1)", "package_ndc": "71335-2889-1", "marketing_start_date": "20251029"}], "brand_name": "Clonidine Hydrochloride", "product_id": "71335-2889_42540d3c-5254-6bc7-e063-6294a90adf98", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "71335-2889", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA202297", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}