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HEXATRIONE

Medically reviewed by Drugs.com. Last updated on Dec 1, 2021.

NDC 59137-570-01

  • 2 mL single-dose ampoule (40 mg/2mL). One ampoule per carton.

20 mg/mL (2 mL Ampoule) - Ampoule Label

20 mg/mL (2 mL Ampoule) - Carton Label

HEXATRIONE 2%
triamcinolone hexacetonide injection, suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:59137-570
Route of Administration INTRA-ARTICULAR DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRIAMCINOLONE HEXACETONIDE (TRIAMCINOLONE ACETONIDE) TRIAMCINOLONE HEXACETONIDE 40 mg in 2 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM HYDROXIDE
SORBITOL SOLUTION 70%
WATER
HYDROCHLORIC ACID
BENZYL ALCOHOL
POLYSORBATE 80
Packaging
# Item Code Package Description
1 NDC:59137-570-01 1 AMPULE in 1 CARTON
1 2 mL in 1 AMPULE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug for use in drug shortage 03/03/2021
Labeler - Medexus Pharma, Inc. (078811131)
Establishment
Name Address ID/FEI Operations
Valdepharm 260128560 manufacture(59137-570)
Medexus Pharma, Inc.

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