Atenolol Scopolamine
Approved
Approval ID
057842c3-d85a-3282-e054-00144ff88e88
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 14, 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.
Atenolol Scopolamine
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69267-101
Product Classification
G
Generic Name
Atenolol Scopolamine
Product Specifications
Route of AdministrationSUBLINGUAL, BUCCAL, TRANSMUCOSAL, ORAL
Effective DateOctober 14, 2014
FDA Product Classification
INGREDIENTS (2)
ATENOLOLActive
Quantity: 25 mg in 25.25 mg
Code: 50VV3VW0TI
Classification: ACTIB
SCOPOLAMINE HYDROBROMIDEActive
Quantity: .25 mg in 25.25 mg
Code: 451IFR0GXB
Classification: ACTIB