Package 43063-925-30

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-925-30
Digits Only 4306392530
Product NDC 43063-925
Description

30 TABLET in 1 BOTTLE, PLASTIC (43063-925-30)

Marketing

Marketing Status
Marketed Since 2019-01-07
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": "415e5e43-7ecc-06d8-e063-6294a90a132b", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884185"], "spl_set_id": ["ea1527a5-4939-4ff7-a827-f88a9113a07d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-925-30)", "package_ndc": "43063-925-30", "marketing_start_date": "20190107"}], "brand_name": "clonidine hydrochloride", "product_id": "43063-925_415e5e43-7ecc-06d8-e063-6294a90a132b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "43063-925", "generic_name": "clonidine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}