Actos
ACTOS (pioglitazone hydrochloride) Tablets
Approved
Approval ID
fd156adc-3174-44da-bff7-eeaef5983f18
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 1, 2010
Manufacturers
FDA
Rebel Distributors Corp.
DUNS: 118802834
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
pioglitazone hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-148
Application NumberNDA021073
Product Classification
M
Marketing Category
C73594
G
Generic Name
pioglitazone hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 1, 2009
FDA Product Classification
INGREDIENTS (1)
pioglitazone hydrochlorideActive
Quantity: 30 mg in 1 1
Code: JQT35NPK6C
Classification: ACTIB
pioglitazone hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-147
Application NumberNDA021073
Product Classification
M
Marketing Category
C73594
G
Generic Name
pioglitazone hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 1, 2009
FDA Product Classification
INGREDIENTS (1)
pioglitazone hydrochlorideActive
Quantity: 15 mg in 1 1
Code: JQT35NPK6C
Classification: ACTIB