FAMOTIDINE injection, solution

Quốc gia: Hoa Kỳ

Ngôn ngữ: Tiếng Anh

Nguồn: NLM (National Library of Medicine)

Thành phần hoạt chất:

FAMOTIDINE (UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8)

Sẵn có từ:

Cantrell Drug Company

INN (Tên quốc tế):

FAMOTIDINE

Thành phần:

FAMOTIDINE 2 mg in 1 mL

Tuyến hành chính:

INTRAVENOUS

Loại thuốc theo toa:

PRESCRIPTION DRUG

Tình trạng ủy quyền:

unapproved drug other

Đặc tính sản phẩm

FAMOTIDINE- FAMOTIDINE INJECTION, SOLUTION
CANTRELL DRUG COMPANY
_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._
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FAMOTIDINE 2 MG/ML IN 0.9% SODIUM CHLORIDE 10 ML SYRINGE
FAMOTIDINE
famotidine injection, solution
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN PRESCRIPTION DRUG
ITE M CODE (SOURCE )
NDC:52533-172
ROUTE OF ADMINISTRATION
INTRAVENOUS
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
FAMO TIDINE (UNII: 5QZO15J2Z8 ) (FAMOTIDINE - UNII:5QZO15J2Z8 )
FAMOTIDINE
2 mg in 1 mL
Cantrell Drug Company
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)
9 mg in 1 mL
MANNITO L (UNII: 3OWL53L36 A)
4 mg in 1 mL
ASPARTIC ACID (UNII: 30 KYC7MIAI)
0 .0 0 5 mg in 1 mL
WATER (UNII: 0 59 QF0 KO0 R)
OTHER INGREDIENTS
INGREDIENT KIND
INGREDIENT NAME
QUANTITY
May co ntain
HYDRO CHLO RIC ACID (UNII: QTT1758 2CB)
May co ntain
SO DIUM HYDRO XIDE (UNII: 55X0 4QC32I)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:52533-172-12
10 mL in 1 SYRINGE, PLASTIC
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
MARKE TING START DATE
MARKE TING END DATE
unappro ved drug o ther
0 6 /11/20 14
LABELER -
Cantrell Drug Company (035545763)
Revised: 6/2014