TOLTRAZURIL powder

United States - English - NLM (National Library of Medicine)

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Active ingredient:
TOLTRAZURIL (UNII: QVZ3IAR3JS) (TOLTRAZURIL - UNII:QVZ3IAR3JS)
Available from:
Darmerica, LLC
Administration route:
NOT APPLICABLE
Authorization status:
Bulk Ingredient For Animal Drug Compounding
Authorization number:
71052-061-05, 71052-061-20, 71052-061-25, 71052-061-26, 71052-061-50

TOLTRAZURIL- toltrazuril powder

Darmerica, LLC

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T oltrazuril

T oltrazuril

TOLTRAZURIL

toltrazuril powder

Product Information

Product T ype

BULK INGREDIENT

Ite m Code (Source )

NDC:710 52-0 6 1

Route of Administration

NOT APPLICABLE

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

TO LTRAZURIL (UNII: QVZ3IAR3JS) (TOLTRAZURIL - UNII:QVZ3IAR3JS)

TOLTRAZURIL

1 g in 1 g

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:710 52-0 6 1-20

10 0 0 g in 1 BOTTLE

0 5/0 1/20 17

2

NDC:710 52-0 6 1-0 5

50 0 0 g in 1 CONTAINER

0 8 /0 2/20 19

3

NDC:710 52-0 6 1-25

25 g in 1 CONTAINER

0 8 /0 2/20 19

4

NDC:710 52-0 6 1-26

250 0 0 g in 1 CONTAINER

0 8 /0 2/20 19

5

NDC:710 52-0 6 1-50

50 0 g in 1 CONTAINER

0 8 /0 2/20 19

Darmerica, LLC

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph

Cita tio n

Marke ting Start

Date

Marke ting End

Date

BULK INGREDIENT FOR ANIMAL DRUG

COMPOUNDING

0 5/0 1/20 17

Labeler -

Darmerica, LLC (080233052)

Revised: 11/2019

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