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