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Medicine

Potassium chloride 1500 mg extended-release tablet

Available on requestPrescription onlyUS FDAGeneric name

Potassium chloride 1500 mg extended-release tablet is a generic prescription medicine for oral use, made by 23 labelers, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Store at room temperature 20° - 25°C (68° - 77°F), excursions permitted to 15°…

Key facts

Active ingredient (INN)
Potassium chloride
Brand
Sold under the generic name
Strength
1500 mg
Dosage form
Extended-release tablet
Route
Oral
Packs
100 tablets, 500 tablets, 1000 tablets and 128 more
Manufacturers
Zydus LifesciencesIndiaAurobindo PharmaIndiaGranules IndiaIndiaCamber PharmaceuticalsIndiaA-S Medication SolutionsAdvagen PharmaUpsher-SmithLaboratoriesSlate Run PharmaceuticalsUpsher-Smith LaboratoriesXLCare Pharmaceuticals23 labelers on the register
Origin register
US FDA, United States
Storage
Store at room temperature 20° - 25°C (68° - 77°F), excursions permitted to 15° - 30°C (59° - 86°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
A12BA01 Potassium chloride
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
20 November 1998
Identifiers
RxCUI 198116, 628953, 2693253 +3DailyMed set ID 8000e242-fe20-4d02-8f7d-97298857cf4c, ace1eb11-b925-405a-b772-58c60b3ca7d4, 099c3a36-f460-4191-80e5-0c4153a5c713 +37NDC 72888-076, 70518-4383, 70771-1600 +37Application ANDA215725, ANDA214452, ANDA210395 +8

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

A sample of 40 packs from 23 labelers. The register lists 131 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
100 tablet, extended release in 1 bottle68382-740-01Zydus LifesciencesIndia3 February 2022
500 tablet, extended release in 1 bottle68382-740-05Zydus LifesciencesIndia3 February 2022
1000 tablet, extended release in 1 bottle68382-740-10Zydus LifesciencesIndia3 February 2022
1000 tablet, extended release in 1 bottle70771-1600-0Zydus LifesciencesIndia3 February 2022
100 tablet, extended release in 1 bottle70771-1600-1Zydus LifesciencesIndia3 February 2022
500 tablet, extended release in 1 bottle70771-1600-5Zydus LifesciencesIndia3 February 2022
100 tablet, extended release in 1 bottle59651-431-01Aurobindo PharmaIndia31 March 2021
500 tablet, extended release in 1 bottle59651-431-05Aurobindo PharmaIndia31 March 2021
90 tablet, extended release in 1 bottle59651-431-90Aurobindo PharmaIndia31 March 2021
100 tablet, extended release in 1 bottle31722-135-01Camber PharmaceuticalsIndia20 January 2021
500 tablet, extended release in 1 bottle31722-135-05Camber PharmaceuticalsIndia20 January 2021
100 tablet, extended release in 1 bottle70010-135-01Granules IndiaIndia30 January 2021
500 tablet, extended release in 1 bottle70010-135-05Granules IndiaIndia30 January 2021
1000 tablet, extended release in 1 bottle70010-135-10Granules IndiaIndia30 January 2021
100 tablet, film coated, extended release in 1 bottle72888-076-01Advagen Pharma25 July 2022
500 tablet, film coated, extended release in 1 bottle72888-076-05Advagen Pharma25 July 2022
1000 tablet, extended release in 1 bottle72888-099-00Advagen Pharma16 June 2023
100 tablet, extended release in 1 bottle72888-099-01Advagen Pharma16 June 2023
100 tablet, film coated, extended release in 1 bottle70436-153-01Slate Run Pharmaceuticals1 February 2020
500 tablet, film coated, extended release in 1 bottle70436-153-02Slate Run Pharmaceuticals1 February 2020
100 tablet, extended release in 1 bottle, plastic24979-232-01Upsher-Smith Laboratories10 April 2023
500 tablet, extended release in 1 bottle, plastic24979-232-02Upsher-Smith Laboratories10 April 2023
1000 tablet, extended release in 1 bottle0832-5325-10Upsher-SmithLaboratories21 June 2019
100 tablet, extended release in 1 bottle0832-5325-11Upsher-SmithLaboratories21 June 2019
500 tablet, extended release in 1 bottle0832-5325-15Upsher-SmithLaboratories21 June 2019
100 tablet, extended release in 1 bottle72865-196-01XLCare Pharmaceuticals4 March 2021
500 tablet, extended release in 1 bottle72865-196-05XLCare Pharmaceuticals4 March 2021
30 tablet, extended release in 1 bottle50090-3700-0A-S Medication Solutions19 October 2018
60 tablet, extended release in 1 bottle, plastic50090-3700-1A-S Medication Solutions26 July 2016
90 tablet, extended release in 1 bottle, plastic50090-3700-2A-S Medication Solutions26 July 2016
30 tablet, extended release in 1 bottle50090-5665-0A-S Medication Solutions15 September 2021
60 tablet, extended release in 1 bottle50090-5665-1A-S Medication Solutions15 September 2021
90 tablet, extended release in 1 bottle50090-5665-2A-S Medication Solutions15 September 2021
30 tablet, extended release in 1 bottle50090-6253-0A-S Medication Solutions2 December 2022
60 tablet, extended release in 1 bottle50090-6253-1A-S Medication Solutions2 December 2022
90 tablet, extended release in 1 bottle50090-6253-2A-S Medication Solutions2 December 2022
30 tablet, extended release in 1 bottle50090-6866-0A-S Medication Solutions4 December 2023
60 tablet, extended release in 1 bottle50090-6866-1A-S Medication Solutions4 December 2023
90 tablet, extended release in 1 bottle50090-6866-2A-S Medication Solutions4 December 2023
90 tablet, extended release in 1 bottle50090-6867-0A-S Medication Solutions4 December 2023

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 25 April 1975Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Alternatives

Other makers and brands of Potassium chloride 1500 mg extended-release tablet.

Compare 1

Other strengths and forms of Potassium chloride

Clinical summary

Potassium chloride is an osmotic laxative indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. MedsAcross supplies Potassium chloride for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Read about Potassium chloride

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need Potassium chloride 1500 mg extended-release tablet for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.