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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

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Chlorthalidone - FDA Drug Approval Details