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