![ATENOLOL SCOPOLAMINE TABLET [TPS]](https://medic.hrt.org//dailymed/images/057842c3-d85a-3282-e054-00144ff88e88/Pill bottle low res.jpg)
| NDC | 69267-101-06, 69267-101-12, 69267-101-24, 69267-101-48 |
| Set ID | 057842c3-d85a-3282-e054-00144ff88e88 |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | TPS |
| Generic Name | |
| Product Class | Anticholinergic, beta-Adrenergic Blocker |
| Product Number | |
| Application Number |
- INSTRUCTIONS FOR USE
Take one tablet sublingually or orally as directed by your physician as needed for symptoms of panic or anxiety.
Do not exceed two tablets per day.
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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
ATENOLOL SCOPOLAMINE TABLET TRITURATE
25 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
ATENOLOL SCOPOLAMINE
atenolol scopolamine tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69267-101 Route of Administration SUBLINGUAL, BUCCAL, TRANSMUCOSAL, ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATENOLOL (UNII: 50VV3VW0TI) (ATENOLOL - UNII:50VV3VW0TI) ATENOLOL 25 mg in 25.25 mg SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB) (SCOPOLAMINE - UNII:DL48G20X8X) SCOPOLAMINE HYDROBROMIDE .25 mg in 25.25 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:69267-101-24 606 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014 2 NDC:69267-101-06 151.5 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014 3 NDC:69267-101-12 303 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014 4 NDC:69267-101-48 1212 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) CloseEstablishment Name Address ID/FEI Business Operations TPS 044805267 manufacture(69267-101)