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MedsAcross

Medicine

Protopam Chloride 1 g/20 mL powder for injection

Pralidoxime · Intramuscular, intravenous, subcutaneous · Baxter Healthcare
Available on requestPrescription onlyUS FDA

Protopam Chloride 1 g/20 mL powder for injection is a prescription medicine containing Pralidoxime for intramuscular, intravenous, subcutaneous use, marketed by Baxter Healthcare, 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°-25°C (68°-77°F), excursions permitted to 15°-30°C (59°-86°F).

Key facts

Active ingredient (INN)
Pralidoxime
Brand
Protopam Chloride
Strength
1 g/20 mL
Dosage form
Powder for injection
Route
Intramuscular, intravenous, subcutaneous
Packs
6 vials
Marketing authorisation holder
Baxter Healthcare
Manufacturer
Baxter Healthcare
Origin register
US FDA, United States
Storage
Store at 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
V03AB04 Pralidoxime
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
10 March 1965
Identifiers
RxCUI 208969, 312576DailyMed set ID 2741d8fd-51c2-46be-880b-99f2b20a6137NDC 60977-141Application NDA014134

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
6 vial, single-dose in 1 package / 20 mL in 1 vial, single-dose60977-141-01Baxter Healthcare10 March 1965

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 11 March 1964Drugs@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

Pralidoxime is a cholinesterase reactivator indicated as an antidote. It is available as powder for injection for intramuscular, intravenous and subcutaneous use. MedsAcross supplies Pralidoxime 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 Pralidoxime

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

Data sources

Need Protopam Chloride 1 g/20 mL powder for 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.