Package 51655-451-25
Brand: clonidine hydrochloride
Generic: clonidine hydrochloridePackage Facts
Identity
Package NDC
51655-451-25
Digits Only
5165545125
Product NDC
51655-451
Description
60 TABLET in 1 BOTTLE, PLASTIC (51655-451-25)
Marketing
Marketing Status
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": "490eece5-957f-26d0-e063-6294a90ae1ae", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["f30324be-47b6-7f54-e053-2995a90a3ad4"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-451-25)", "package_ndc": "51655-451-25", "marketing_start_date": "20221206"}], "brand_name": "Clonidine hydrochloride", "product_id": "51655-451_490eece5-957f-26d0-e063-6294a90ae1ae", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "51655-451", "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": ".3 mg/1"}], "application_number": "ANDA070923", "marketing_category": "ANDA", "marketing_start_date": "20221206", "listing_expiration_date": "20271231"}