Prescription Drug Information: Succinylcholine Chloride (Page 3 of 3)

How Supplied

Succinylcholine chloride injection, USP is supplied as a clear, colorless solution in the following concentrations and packages:

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Refrigeration of the undiluted agent will assure full potency until expiration date. All units carry a date of expiration.

Store in refrigerator 2° to 8°C (36° to 46°F). The multi-dose vials are stable for up to 14 days at room temperature without significant loss of potency.

Manufactured by:
RAFARM S.A., Thesi Pousi-Hatzi, Agiou Louka, 19002,
Paiania, Attiki, Greece

Distributed by:
Breckenridge Pharmaceutical, Inc.Berlin, CT 06037

Revised: 10/2019

30804998

Sample Package Label

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SUCCINYLCHOLINE CHLORIDE succinylcholine chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0404-9960(NDC:51991-964)
Route of Administration INTRAVENOUS, INTRAMUSCULAR DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SUCCINYLCHOLINE CHLORIDE (SUCCINYLCHOLINE) SUCCINYLCHOLINE CHLORIDE 20 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
METHYLPARABEN 1.8 mg in 1 mL
PROPYLPARABEN 0.2 mg in 1 mL
SODIUM HYDROXIDE
HYDROCHLORIC ACID
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0404-9960-10 1 VIAL, MULTI-DOSE in 1 BAG contains a VIAL, MULTI-DOSE
1 10 mL in 1 VIAL, MULTI-DOSE This package is contained within the BAG (0404-9960-10)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA212638 01/12/2022
Labeler — Henry Schein, Inc. (012430880)

Revised: 01/2022 Henry Schein, Inc.

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