Chlorthalidone
Chlorthalidone
Approved
Approval ID
c10e3a16-d94f-442f-9303-4ded0adaecc1
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 16, 2010
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
chlorthalidone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-671
Application NumberANDA086831
Product Classification
M
Marketing Category
C73584
G
Generic Name
chlorthalidone
Product Specifications
Route of AdministrationORAL
Effective DateNovember 16, 2009
FDA Product Classification
INGREDIENTS (7)
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
CHLORTHALIDONEActive
Quantity: 25 mg in 1 1
Code: Q0MQD1073Q
Classification: ACTIB
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT