MedPath

Telmisartan

Telmisartan

Approved
Approval ID

b88dc14d-24ce-4569-a57d-af3334e4fa90

Product Type

BULK INGREDIENT - ANIMAL DRUG

Effective Date

Aug 1, 2025

Manufacturers
FDA

AX Pharmaceutical Corp

DUNS: 204011316

Products 1

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

Telmisartan

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code73377-036
Product Classification
G
Generic Name
Telmisartan
Product Specifications
Route of AdministrationNOT APPLICABLE
Effective DateAugust 1, 2025
FDA Product Classification

INGREDIENTS (1)

TELMISARTANActive
Quantity: 1 g in 1 g
Code: U5SYW473RQ
Classification: ACTIB

Drug Labeling Information

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOINC: 51945-4Updated: 8/1/2025

Telmisartan

image descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage description

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Telmisartan - FDA Drug Approval Details