PROPRANOLOL SCOPOLAMINE tablet

Propranolol Scopolamine by

Drug Labeling and Warnings

Propranolol Scopolamine by is a Prescription medication manufactured, distributed, or labeled by TPS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INSTRUCTIONS FOR USE

Take one tablet orally as directed by your physician as needed for symptoms of panic or anxiety.

Do not exceed two tablets per day.

PRINCIPAL DISPLAY PANEL

TPS LLC

3524 DECATUR HWY FULTONDALE, AL 35068

877-608-4995 1-877-608-4995 BT9752747

Caution: Federal law prohibits transfer of this drug to any other person than patient for whom prescribed

Rx 263095 Jack Doe/Dr. Jane Doe MD

JOHN DOE

123 MAIN ST AUBURN, AL 12345

PROPRANOLOL SCOPOLAMINE TABLET TRITURATE

40 MG/0.5 MG

48 TABS Lot# Exp

Take 1 tablet sublingually or orally as directed by your physician as needed for symptoms of panic or anxiety.

Do not exceed 2 tablets per day

PH No refills authorized 10/8/2014

Pill bottle low res.jpg

INGREDIENTS AND APPEARANCE

PROPRANOLOL SCOPOLAMINE 
propranolol scopolamine tablet

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 69267-202
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V) (PROPRANOLOL - UNII:9Y8NXQ24VQ)	PROPRANOLOL HYDROCHLORIDE	40 mg  in 40.5 mg
SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB) (SCOPOLAMINE - UNII:DL48G20X8X)	SCOPOLAMINE HYDROBROMIDE	.5 mg  in 40.5 mg

Product Characteristics
Color	white	Score	no score
Shape	ROUND (THE DIAMETER DEPENDS ON DIES)	Size	5mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69267-202-06	243 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2014
2	NDC: 69267-202-12	486 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2014
3	NDC: 69267-202-24	972 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2014
4	NDC: 69267-202-48	1944 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/01/2014

Labeler - TPS (044805267)

Establishment
Name	Address	ID/FEI	Business Operations
TPS		044805267	manufacture(69267-202)