MedPath

Propranolol Scopolamine

Approved
Approval ID

0579a12e-690b-3fa0-e054-00144ff88e88

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 15, 2014

Manufacturers
FDA

TPS

DUNS: 044805267

Products 1

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

Propranolol Scopolamine

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code69267-201
Product Classification
G
Generic Name
Propranolol Scopolamine
Product Specifications
Route of AdministrationORAL
Effective DateOctober 15, 2014
FDA Product Classification

INGREDIENTS (2)

SCOPOLAMINE HYDROBROMIDEActive
Quantity: .25 mg in 20.25 mg
Code: 451IFR0GXB
Classification: ACTIB
PROPRANOLOL HYDROCHLORIDEActive
Quantity: 20 mg in 20.25 mg
Code: F8A3652H1V
Classification: ACTIB

MedPath

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

© 2025 MedPath, Inc. All rights reserved.

Propranolol Scopolamine - FDA Drug Approval Details