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NDC 70934-0851-30 Clonidine hydrochloride 0.1 mg/1 Details

Clonidine hydrochloride 0.1 mg/1

Clonidine hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is CLONIDINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Clonidine tablets (Catapres) are used alone or in combination with other medications to treat high blood pressure. Clonidine extended-release (long-acting) tablets (Kapvay) are used alone or in combination with other medications as part of a treatment program to control symptoms of attention deficit hyperactivity disorder (ADHD; more difficulty focusing, controlling actions, and remaining still or quiet than other people who are the same age) in children. Clonidine is in a class of medications called centrally acting alpha-agonist hypotensive agents. Clonidine treats high blood pressure by decreasing your heart rate and relaxing the blood vessels so that blood can flow more easily through the body. Clonidine extended-release tablets may treat ADHD by affecting the part of the brain that controls attention and impulsivity. High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.

Related Packages: 70934-0851-30
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Clonidine

Product Information

NDC	70934-0851
Product ID	70934-851_f1773d46-06f4-3f6b-e053-2a95a90a281a
Associated GPIs	36201010100305
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Clonidine hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Clonidine hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	0.1
Active Ingredient Units	mg/1
Substance Name	CLONIDINE HYDROCHLORIDE
Labeler Name	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Pharmaceutical Class	Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA070925
Listing Certified Through	n/a

Package

NDC 70934-0851-30 (70934085130)

Pricing Information	N/A
NDC Package Code	70934-851-30
Billing NDC	70934085130
Package	30 TABLET in 1 BOTTLE, PLASTIC (70934-851-30)
Marketing Start Date	2021-04-12
NDC Exclude Flag	N