NDC | 69267-201-06, 69267-201-12, 69267-201-24, 69267-201-48 |
Set ID | 0579a12e-690b-3fa0-e054-00144ff88e88 |
Category | HUMAN PRESCRIPTION DRUG LABEL |
Packager | TPS |
Generic Name | |
Product Class | Anticholinergic |
Product Number | |
Application Number |
- INSTRUCTIONS FOR USE
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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
20 MG/0.25 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
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INGREDIENTS AND APPEARANCE
PROPRANOLOL SCOPOLAMINE
propranolol scopolamine tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69267-201 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB) (SCOPOLAMINE - UNII:DL48G20X8X) SCOPOLAMINE HYDROBROMIDE .25 mg in 20.25 mg PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V) (PROPRANOLOL - UNII:9Y8NXQ24VQ) PROPRANOLOL HYDROCHLORIDE 20 mg in 20.25 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:69267-201-06 121.5 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014 2 NDC:69267-201-12 243 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014 3 NDC:69267-201-24 486 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014 4 NDC:69267-201-48 972 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(69267-201)