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Medicine

Normosol-m And Dextrose 50 g/210 mg/1280 mg/2340 mg per 1000 mL injection

Available on requestPrescription onlyUS FDA

Normosol-m And Dextrose 50 g/210 mg/1280 mg/2340 mg per 1000 mL injection is a prescription medicine containing Dextrose, Magnesium acetate, Potassium acetate and Sodium chloride for intravenous use, marketed by ICU Medical, 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 20 to 25°C (68 to 77°F).

Key facts

Active ingredient (INN)
Dextrose, Magnesium acetate, Potassium acetate and Sodium chloride
Brand
Normosol-m And Dextrose
Strength
50 g/210 mg/1280 mg/2340 mg per 1000 mL
Dosage form
Injection
Route
Intravenous
Packs
12 pouches of 1000 mL
Marketing authorisation holder
ICU Medical
Manufacturer
ICU Medical
Origin register
US FDA, United States
Storage
Store at 20 to 25°C (68 to 77°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
8 February 2021
Identifiers
RxCUI 801005, 801009DailyMed set ID aba60c84-94d9-46d0-bdbb-25e0c4e8cc41NDC 0990-7965Application NDA017610

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

PackCodeLabelerMarketed since
12 pouch in 1 case / 1 bag in 1 pouch / 1000 mL in 1 bag0990-7965-09ICU Medical8 February 2021

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 13 August 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

Clinical summary

Dextrose, Magnesium acetate, Potassium acetate and Sodium chloride is a fixed-dose combination of an osmotic laxative, a calculi dissolution agent and a potassium salt. MedsAcross supplies Dextrose, Magnesium acetate, Potassium acetate and Sodium 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 Dextrose, Magnesium acetate, Potassium acetate and Sodium chloride

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

Data sources

Need Normosol-m And Dextrose 50 g/210 mg/1280 mg/2340 mg per 1000 mL injection 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.