MedPath

Aminophylline

Approved
Approval ID

6bca324f-6999-4c16-e053-2a91aa0aee45

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

May 30, 2023

Manufacturers
FDA

Medical Purchasing Solutions, LLC

DUNS: 601458529

Products 1

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

Aminophylline

PRODUCT DETAILS

NDC Product Code71872-7060
Application NumberANDA087242
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateMay 30, 2023
Generic NameAminophylline

INGREDIENTS (3)

WATERInactive
Code: 059QF0KO0R
Classification: IACT
ETHYLENEDIAMINEInactive
Code: 60V9STC53F
Classification: IACT
AMINOPHYLLINE DIHYDRATEActive
Quantity: 25 mg in 1 mL
Code: C229N9DX94
Classification: ACTIB

MedPath

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

© 2025 MedPath, Inc. All rights reserved.

Aminophylline - FDA Drug Approval Details