CLONIDINE HYDROCHLORIDE
CLONIDINE HYDROCHLORIDE USP Oral Antihypertensive Tablets of 0.1, 0.2 and 0.3 mg
Approved
Approval ID
81dd2c3f-724d-44c3-ab0e-f0e111958741
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 30, 2010
Manufacturers
FDA
Blenheim Pharmacal, Inc.
DUNS: 171434587
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
clonidine hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code10544-158
Application NumberANDA070924
Product Classification
M
Marketing Category
C73584
G
Generic Name
clonidine hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateJune 30, 2010
FDA Product Classification
INGREDIENTS (1)
clonidine hydrochlorideActive
Quantity: 0.2 mg in 1 1
Code: W76I6XXF06
Classification: ACTIB