MedPath

Trepoxen-250

Trepoxen-250

Approved
Approval ID

c957df9a-eb66-432f-a280-9cd74389d667

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 1, 2011

Manufacturers
FDA

Physician Therapeutics LLC

DUNS: 931940964

Products 1

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

NAPROXEN,HISTIDINE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code68405-016
Product Classification
G
Generic Name
NAPROXEN,HISTIDINE
Product Specifications
Effective DateAugust 10, 2011
FDA Product Classification

MedPath

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

© 2025 MedPath, Inc. All rights reserved.

Trepoxen-250 - FDA Drug Approval Details