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Truemed Group LLC

TELMISARTAN HYDROCHLOROTHIAZIDE

Approved
Approval ID

e5fb55b6-5cdc-b9ed-e053-2995a90a37c3

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 11, 2022

Manufacturers
FDA

Truemed Group LLC

DUNS: 004154534

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

TELMISARTAN-HYDROCHLOROTHIAZIDE

PRODUCT DETAILS

NDC Product Code82922-037
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationORAL
Effective DateAugust 11, 2022
Generic NameTELMISARTAN-HYDROCHLOROTHIAZIDE

INGREDIENTS (2)

HYDROCHLOROTHIAZIDEActive
Quantity: 12.5 mg in 1 1
Code: 0J48LPH2TH
Classification: ACTIB
TELMISARTANActive
Quantity: 80 mg in 1 1
Code: U5SYW473RQ
Classification: ACTIB
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