Equisul-SDT: Product Information (Page 3 of 3)

PRINCIPAL DISPLAY PANEL — 280 mL Bottle Label with draw-off cap

NDC 51072-020-03

EQUISUL-SDT®

(Sulfadiazine/Trimethoprim)

Antimicrobial

Oral Suspension

400 mg/mL

Approved by FDA under NADA # 141-360

CAUTION: Federal law (USA) restricts this drug to use by or on the order of a licensed veterinarian.

For use in horses only.

280 mL

REORDER No: 28003

IN 50-1346 01/2021

aurora pharmaceutical®

PRINCIPAL DISPLAY PANEL -- 280 mL Bottle Label with draw-off cap
(click image for full-size original)
EQUISUL-SDT sulfadiazine and trimethoprim suspension
Product Information
Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:51072-020
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SULFADIAZINE (SULFADIAZINE) SULFADIAZINE 333 mg in 1 mL
TRIMETHOPRIM (TRIMETHOPRIM) TRIMETHOPRIM 67 mg in 1 mL
Product Characteristics
Color WHITE Score
Shape Size
Flavor APPLE Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51072-020-00 900 mL in 1 BOTTLE None
2 NDC:51072-020-01 135 mL in 1 BOTTLE None
3 NDC:51072-020-02 560 mL in 1 BOTTLE None
4 NDC:51072-020-03 280 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NADA NADA141360 08/05/2013
Labeler — Aurora Pharmaceutical, Inc. (832848639)
Establishment
Name Address ID/FEI Operations
Aurora Pharmaceutical, Inc. 832848639 MANUFACTURE

Revised: 12/2021 Aurora Pharmaceutical, Inc.

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