CHLORURE DE POTASSIUM PROAMP- potassium chloride injection, solution, concentrate 
Laboratoire Aguettant

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Potassium Chloride for Injection Concentrate, USP

La Jolla
Pharmaceutical

AGUETTANT
ESSENTIAL
MEDICINES

Important Prescribing Information

Subject: Temporary importation of Potassium Chloride Proamp® 0.15 g/mL (equivalent to 2 mEq/mL), concentrate for solution for infusion to address drug shortage

June, 2018

Dear Healthcare Professional,

Due to the critical shortage of Potassium Chloride for Injection Concentrate 2 mEq/mL, USP in the United States (U.S.) market, Laboratoire Aguettant (Aguettant) is coordinating with the U.S. Food and Drug Administration (FDA) to increase the availability of Potassium Chloride for Injection. Aguettant has initiated temporary importation of its Potassium Chloride Proamp® 0.15 g/mL (equivalent to 2 mEq/mL) concentrate for solution for infusion. This product is manufactured and marketed in France by Aguettant.

Given the scale of this shortage, FDA is coordinating with several firms to import Potassium Chloride for Injection 2 mEq/mL. At this time, however, no other entity except La Jolla Pharmaceutical Company is authorized by the FDA to import or distribute Aguettant's Potassium Chloride Proamp® 0.15 g/mL (equivalent to 2 mEq/mL) concentrate for solution for infusion. FDA has not approved Aguettant's Potassium Chloride Proamp® 0.15 g/mL concentrate for solution for infusion, but allows its temporary importation into the United States. You may be provided with additional letters for other imported products you receive. Please read each letter in its entirety because each letter may contain different, product-specific information.

Effective immediately, and during this temporary period, Aguettant will offer the following presentation of Potassium Chloride for Injection:

Product name and descriptionSizePack factorNDC Number
Potassium Chloride Proamp® 0.15 g/mL, concentrate for solution for infusion (equivalent to 2 mEq/mL)10 mL50 ampules per box60710-015-50

There are key differences between the labeling of the FDA approved Potassium Chloride for Injection 2 mEq/mL products and Aguettant's imported Potassium Chloride Proamp® 0.15 g/mL.

It is important to note the following:

A side by side comparison of the key differences in the labeling between the FDA-approved product and the imported product is displayed in the product comparison table at the end of this letter.

Please refer to the package insert for the FDA-approved Potassium Chloride for Injection Concentrate, USP drug product for full prescribing information.

To order or if you have questions about Aguettant's Potassium Chloride Proamp® 0.15 g/mL ampules, please contact La Jolla Pharmaceutical Company at 1-800-651-3861.

To report an adverse event concerning the imported Potassium Chloride Proamp® 0.15 g/mL ampules, please contact La Jolla Pharmaceutical Company at 1-800-651-3861. Adverse events or quality problems experienced with the use of the Potassium Chloride Proamp® 0.15 g/mL ampules may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax:

If you have any questions about the information contained in this letter or use of Aguettant's Potassium Chloride Proamp® 0.15 g/mL ampules, please contact La Jolla's Medical Information Contact Center (MICC) at 1-800-651-3861.

Sincerely,

Jérôme JOLY
Laboratoire Aguettant
Director, Global QP
Cécile BAILLY
Laboratoire Aguettant
Medical Director
George F. Tidmarsh, MD, PhD
Chief Executive Officer
La Jolla Pharmaceutical Company
Doranne Frano
Vice President, Regulatory Affairs
La Jolla Pharmaceutical Company

PRODUCT COMPARISON TABLE

Import ProductU.S. Marketed Product
AGUETTANTHOSPIRA
PresentationFigureFigure
Drug NamePotassium chloride Proamp® 0.15 g/mL, concentrate for solution for infusionPotassium Chloride for Injection Concentrate, USP
Active Ingredient ConcentrationPotassium: 2.012 mmol/mL
Equivalent to: (2 mEq K+/mL)
(149 mg/mL)
Each mL contains potassium chloride, 2 mEq (149 mg)
Unit Volume / Volume10 ml polypropylene ampules
The ampules are made by polypropylene compliant to the 3.1.6. European pharmacopoeia monograph.
They are formed through blow fill seal process and are terminally sterilized at 121°C, assuring a maximal level of sterility of the contained solution.
5 mL single dose vials
Semi-rigid plastic vials fabricated from a specially formulated polyolefin.
Indication and UsageConcentrate for solution for infusion administered to patients suffering from low potassium blood levels (hypokalemia). Potassium is naturally present in body fluids and is needed for normal body function. It can also be used as a potassium supply for patients who are unable to be fed orally and receive total parenteral nutrition.Potassium Chloride for Injection Concentrate, USP is indicated in the treatment of potassium deficiency states when oral replacement is not feasible.

PRINCIPAL DISPLAY PANEL - 10 mL Ampule Label

POTASSIUM chlorure PROAMP®
1,5 g - 10 mL
0,15 g/mL
2,012 mmol/mL d'ion K+
Solution à diluer pour perfusion - IV
A diluer avant utilisation

K

15%

PRINCIPAL DISPLAY PANEL - 10 mL Ampule Label

PRINCIPAL DISPLAY PANEL - 10 mL Ampule Box

CHLORURE DE POTASSIUM PROAMP® 0, 15 g/mL AGUETTANT
POTASSIUM CHLORIDE

CAUTION

Potassium Chloride for Injection
Concentrate

Each ampule contains 20 mEq/10 mL
(2 mEq/mL)

0,15 g/mL = 2 mEq/mL

Must be diluted before use

IV use

AGUETTANT

50
polypropylene ampoules

1,5 g
10 mL

PRINCIPAL DISPLAY PANEL - 10 mL Ampule Box
CHLORURE DE POTASSIUM PROAMP 
potassium chloride injection, solution, concentrate
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:60710-015
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
potassium chloride (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) potassium chloride0.15 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:60710-015-5050 in 1 BOX07/31/2018
110 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug for use in drug shortage07/31/2018
Labeler - Laboratoire Aguettant (267584998)
Establishment
NameAddressID/FEIBusiness Operations
Laboratoire Aguettant271085545MANUFACTURE(60710-015) , ANALYSIS(60710-015) , LABEL(60710-015) , PACK(60710-015) , STERILIZE(60710-015) , RELABEL(60710-015)

Revised: 8/2018
Document Id: d9d09d39-83c2-4447-8171-22ef87173883
Set id: d7d402fb-ac55-4f53-91e7-345df18c2d53
Version: 2
Effective Time: 20180813
 
Laboratoire Aguettant