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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
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Chlorthalidone - FDA Approval | MedPath