Страна: Соединенные Штаты
Язык: английский
Источник: NLM (National Library of Medicine)
SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB) (SCOPOLAMINE - UNII:DL48G20X8X), PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V) (PROPRANOLOL - UNII:9Y8NXQ24VQ)
TPS
ORAL
PRESCRIPTION DRUG
Take one tablet orally as directed by your physician as needed for symptoms of panic or anxiety. Do not exceed two tablets per day.
unapproved drug other
PROPRANOLOL SCOPOLAMINE- PROPRANOLOL SCOPOLAMINE TABLET TPS _Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been_ _approved by FDA. For further information about unapproved drugs, click here._ ---------- Take one tablet orally as directed by your physician as needed for symptoms of panic or anxiety. Do not exceed two tablets per day. 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 PROPRANOLOL SCOPOLAMINE propranolol scopolamine tablet PRODUCT INFORMATION PRODUCT T YPE HUMAN PRESCRIPTION DRUG ITE M CODE (SOURCE ) NDC:6 9 26 7-20 1 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH SCO PO LAMINE HYDRO BRO MIDE (UNII: 451IFR0 GXB) (SCOPOLAMINE - UNII:DL48 G20 X8 X) SCOPOLAMINE HYDROBROMIDE .25 mg in 20 .25 mg PRO PRANO LO L HYDRO CHLO RIDE (UNII: F8 A36 52H1V) (PROPRANOLOL - UNII:9 Y8 NXQ24VQ) PROPRANOLOL HYDROCHLORIDE 20 mg in 20 .25 mg PRODUCT CHARACTERISTICS COLOR white S CORE no sco re S HAP E ROUND (THE DIAMETER DEPENDS ON DIES) S IZ E 5mm FLAVOR IMPRINT CODE CONTAINS PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:6 9 26 7-20 1- 0 6 121.5 mg in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n Pro duc t 10 /0 1/20 14 2 NDC:6 9 26 7-20 1- 12 243 mg in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n Pro duc t 10 /0 1/20 14 3 NDC:6 9 26 7-20 1- 24 48 6 mg in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n Pro duc t 10 /0 1/20 14 4 NDC:6 9 26 7-20 1- 48 9 72 mg in 1 BOTTLE, PLASTIC; Type Прочитать полный документ