Chlorthalidone
Chlorthalidone Tablets, USP VistaPharm, Inc.
Approved
Approval ID
a125d976-4574-33cd-e053-2995a90a834b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 7, 2022
Manufacturers
FDA
NuCare Pharmaceuticals,Inc.
DUNS: 010632300
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Chlorthalidone
PRODUCT DETAILS
NDC Product Code68071-5219
Application NumberANDA211063
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateFebruary 7, 2022
Generic NameChlorthalidone
INGREDIENTS (6)
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A CORNInactive
Code: AG9B65PV6B
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
CHLORTHALIDONEActive
Quantity: 25 mg in 1 1
Code: Q0MQD1073Q
Classification: ACTIB