Propranolol Scopolamine

Product NDC

69267-201

11-digit product format

692670201

Labeler code

69267

Product ID

69267-201_0579a12e-690c-3fa0-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Propranolol Scopolamine

Dosage form

TABLET

Route

ORAL

Labeler

TPS

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2014-10-01

Marketing end

0000-00-00

Substance

SCOPOLAMINE HYDROBROMIDE; PROPRANOLOL HYDROCHLORIDE

Active strength

0 mg/20.25mg; mg/20.25mg

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record