Package 51655-962-52

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-962-52
Digits Only 5165596252
Product NDC 51655-962
Product ID 51655-962_4974a59a-10c1-4b0c-e063-6294a90af79b
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-962-52)

Marketing

Marketing Status
Marketed Since 2022-04-15
Brand clonidine hydrochloride
Generic clonidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Clonidine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4974a59a-10c1-4b0c-e063-6294a90af79b", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884185"], "spl_set_id": ["df77e732-9765-ee5c-e053-2a95a90abc92"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-962-52)", "package_ndc": "51655-962-52", "marketing_start_date": "20220415"}], "brand_name": "Clonidine hydrochloride", "product_id": "51655-962_4974a59a-10c1-4b0c-e063-6294a90af79b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "51655-962", "generic_name": "Clonidine hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA070924", "marketing_category": "ANDA", "marketing_start_date": "20220415", "listing_expiration_date": "20271231"}