Package 51655-353-52

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-353-52
Digits Only 5165535352
Product NDC 51655-353
Product ID 51655-353_48eb5573-d143-de2e-e063-6294a90a0a95
Description

30 TABLET in 1 BOTTLE, DISPENSING (51655-353-52)

Marketing

Marketing Status
Marketed Since 2015-02-25
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": "48eb5573-d143-de2e-e063-6294a90a0a95", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["66dc3cf0-d6bd-436c-9a7f-7477575b3260"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, DISPENSING (51655-353-52)", "package_ndc": "51655-353-52", "marketing_start_date": "20150225"}], "brand_name": "Clonidine Hydrochloride", "product_id": "51655-353_48eb5573-d143-de2e-e063-6294a90a0a95", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "51655-353", "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": ".1 mg/1"}], "application_number": "ANDA070974", "marketing_category": "ANDA", "marketing_start_date": "20150225", "listing_expiration_date": "20271231"}