AX PHARMACEUTICAL CORP- tolazoline hydrochloride powder

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

TOLAZOLINE HYDROCHLORIDE (UNII: E669Z6S1JG) (TOLAZOLINE - UNII:CHH9H12AQ3)

Available from:

AX Pharmaceutical Corp

INN (International Name):

TOLAZOLINE HYDROCHLORIDE

Composition:

TOLAZOLINE 495 g in 500 g

Administration route:

NOT APPLICABLE

Authorization status:

Bulk Ingredient For Animal Drug Compounding

Summary of Product characteristics

AX PHARMACEUTICAL CORP- TOLAZOLINE HYDROCHLORIDE POWDER
AX PHARMACEUTICAL CORP
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AX PHARMACEUTICAL CORP
tolazoline hydrochloride powder
AX Pharmaceutical Corp
PRODUCT INFORMATION
PRODUCT T YPE
BULK INGREDIENT
ITE M CODE (SOURCE )
NDC:6 2157-473
ROUTE OF ADMINISTRATION
NOT APPLICABLE
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
TO LAZO LINE HYDRO CHLO RIDE (UNII: E6 6 9 Z6 S1JG) (TOLAZOLINE -
UNII:CHH9 H12AQ3)
TOLAZOLINE
49 5 g in 50 0 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PRODUCT CHARACTERISTICS
COLOR
white
S CORE
S HAP E
S IZ E
FLAVOR
IMPRINT CODE
CONTAINS
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:6 2157-473-0 1
50 0 g in 1 JAR
0 8 /22/20 17
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH
CITA TIO N
MARKE TING START
DATE
MARKE TING END
DATE
bulk ingredient fo r animal drug
c o mpo unding
0 8 /22/20 17
LABELER -
AX Pharmaceutical Corp (202924858)
ESTABLISHMENT
NAME
AD D RE S S
ID/FEI
BUSINE SS OPE RATIONS
AX Pharmaceutical Co rp
20 29 248 58
repack(6 2157-473) , relabel(6 2157-473)
Revised: 8/2017