clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-353
Product ID 51655-353_48eb5573-d143-de2e-e063-6294a90a0a95
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070974
Listing Expiration 2027-12-31
Marketing Start 2015-02-25

Pharmacologic Class

Classes
adrenergic alpha2-agonists [moa] central alpha-2 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655353
Hyphenated Format 51655-353

Supplemental Identifiers

RxCUI
884173
UNII
W76I6XXF06

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name clonidine hydrochloride (source: ndc)
Generic Name clonidine hydrochloride (source: ndc)
Application Number ANDA070974 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, DISPENSING (51655-353-52)
source: ndc

Packages (1)

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

Ingredients (1)

clonidine hydrochloride (.1 mg/1)

Linked Drug Pages (1)

Clonidine Hydrochloride ndc-match (0.9)

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"}