MedPath

Theraproxen-500

Theraproxen-500

Approved
Approval ID

701b69d8-cce8-42de-a770-96020c1a870a

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, .GAMMA.-AMINOBUTYRIC ACID

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code68405-118
Product Classification
G
Generic Name
NAPROXEN, .GAMMA.-AMINOBUTYRIC ACID
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.

Theraproxen-500 - FDA Drug Approval Details