CLONIDINE HYDROCHLORIDE
CLONIDINE HYDROCHLORIDE USP Oral Antihypertensive Tablets of 0.1 mg
Approved
Approval ID
29283327-3a8a-486d-a9fc-ba5cdc91a09b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 18, 2010
Manufacturers
FDA
Contract Pharmacy Services-PA
DUNS: 945429777
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 Code67046-095
Application NumberANDA070925
Product Classification
M
Marketing Category
C73584
G
Generic Name
clonidine hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateApril 23, 2010
FDA Product Classification
INGREDIENTS (1)
clonidine hydrochlorideActive
Quantity: 0.1 mg in 1 1
Code: W76I6XXF06
Classification: ACTIB