Potassium Chloride for Injection Concentrate, USP

Manufacturer
Laboratoire Aguettant
Effective date
2018-08-13
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:26:12

Label at a glance#

ProductChlorure de potassium Proamp
Active ingredientpotassium chloride
Label structure3 sections

Label contents#

Full prescribing information#

HEALTH CARE PROVIDER LETTER SECTION

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:

  • Aguettant's product is labeled Potassium Chloride Proamp® 0,15 g/mL which means 0.15 g/mL in the U.S. and is equal to 2 mEq/mL of potassium chloride. We have affixed the following sticker with this information on the carton for the imported product.
    FigureFigure
  • The ampule label of Aguettant's product is in French without English translation. However, the carton and the prescribing information for Aguettant's product is translated into English. Institutions should develop a strategy, which may include labeling the ampules with key information, to ensure safe use of the product.
  • Aguettant's product does not contain a barcode. Institutions should manually input the product into their systems. Alternative procedures should be followed to assure that the correct drug product is being used and administered to individual patients.
  • Inspect the solution visually for particulate matter and discoloration prior to administration.
  • The imported product is packaged in polypropylene 10 mL ampules. To use the ampule, hold it upright, twist off the cap, and withdraw the solution using a syringe.

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
PresentationFigureFigureFigureFigure
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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 Label

PRINCIPAL DISPLAY PANEL - 10 mL Ampule Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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
PRINCIPAL DISPLAY PANEL - 10 mL Ampule Box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1860136potassium chloride 20 MEQ in 10 ML InjectionPSN2
186013610 ML potassium chloride 2 MEQ/ML InjectionSCD2
186013610 ML K+ Chloride 2 MEQ/ML InjectionSY2
186013610 ML Pot Chloride 2 MEQ/ML InjectionSY2
1860136potassium chloride 14.9 % per 10 ML InjectionSY2
1860136potassium chloride 20 MEQ per 10 ML InjectionSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
POTASSIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
95250459-30e4-45c1-b08a-993044f49109Product name220250805
d9771140-739b-484b-ae64-b79528ff1211Product name320250801
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60710-015-502020-01-31C16284748780-19d75b9d0-0a99-f424-e053-dadaa90a57cePotassium Chloride for Injection Concentrate, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60710-015-50Chlorure de potassium Proamp50 in 1 BOXINJECTION, SOLUTION, CONCENTRATE502
60710-015-50Chlorure de potassium Proamp10 mL in 1 AMPULEINJECTION, SOLUTION, CONCENTRATE102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60710-015CHLORURE DE POTASSIUM PROAMP (POTASSIUM CHLORIDE) INJECTION, SOLUTION, CONCENTRATE [LABORATOIRE AGUETTANT]2Legacy NDC, 2 package rows20180815_d7d402fb-ac55-4f53-91e7-345df18c2d53.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60710-015-50ML - Milliliter60710-0154376ec6c-b533-4ab7-879f-af3b1dad1f7f12018-10-11

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60710-01560710-015-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
potassium chloride660YQ98I10ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d9d09d39-83c2-4447-8171-22ef87173883d7d402fb-ac55-4f53-91e7-345df18c2d532018-08-13Exact identifier
spl id: d9d09d39-83c2-4447-8171-22ef87173883
spl set id: d7d402fb-ac55-4f53-91e7-345df18c2d53

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.