SELEGILINE HYDROCHLORIDE powder

Pays: États-Unis

Langue: anglais

Source: NLM (National Library of Medicine)

Ingrédients actifs:

SELEGILINE HYDROCHLORIDE (UNII: 6W731X367Q) (SELEGILINE HYDROCHLORIDE - UNII:6W731X367Q)

Disponible depuis:

AX Pharmaceutical Corp

Mode d'administration:

NOT APPLICABLE

Statut de autorisation:

Bulk Ingredient For Animal Drug Compounding

Résumé des caractéristiques du produit

SELEGILINE HYDROCHLORIDE- SELEGILINE HYDROCHLORIDE POWDER
AX PHARMACEUTICAL CORP
----------
SELEGILINE HYDROCHLORIDE
SELEGILINE HYDROCHLORIDE
SELEGILINE HYDROCHLORIDE
selegiline hydrochloride powder
PRODUCT INFORMATION
PRODUCT T YPE
BULK INGREDIENT
ITE M CODE (SOURCE )
NDC:73377-0 12
ROUTE OF ADMINISTRATION
NOT APPLICABLE
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SELEGILINE HYDRO CHLO RIDE (UNII: 6 W731X36 7Q) (SELEGILINE
HYDROCHLORIDE -
UNII:6 W731X36 7Q)
SELEGILINE
HYDROCHLORIDE
1 g in 1 g
AX Pharmaceutical Corp
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:73377-0 12-0 1
50 0 g in 1 JAR
0 2/0 4/20 20
2
NDC:73377-0 12-0 2
10 0 g in 1 JAR
0 3/0 6 /20 20
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 2/0 4/20 20
LABELER -
AX Pharmaceutical Corp (204011316)
ESTABLISHMENT
NAME
AD D RE S S
ID/FEI
BUSINE SS OPE RATIONS
AX Pharmaceutical Co rp
20 40 11316
repack(73377-0 12) , relabel(73377-0 12)
Revised: 2/2020