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Medicine

Erythromycin 200 mg/5 mL powder for oral suspension

Erythromycin · Oral
Available on requestPrescription onlyUS FDAGeneric name

Erythromycin 200 mg/5 mL powder for oral suspension is a generic prescription medicine for oral use, made by 3 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 erythromycin ethylsuccinate for oral suspension, USP 200 mg/5 mL and…

Key facts

Active ingredient (INN)
Erythromycin
Brand
Sold under the generic name
Strength
200 mg/5 mL
Dosage form
Powder for oral suspension
Route
Oral
Packs
100 mL
Manufacturers
Cadila PharmaceuticalsIndiaBryant Ranch PrepackKanchan Healthcare
Origin register
US FDA, United States
Storage
Store erythromycin ethylsuccinate for oral suspension, USP 200 mg/5 mL and erythromycin ethylsuccinate for oral suspension, USP 400 mg/5 mL, prior to mixing, below 86°F (30°C). After reconstitution, erythromycin ethylsuccinate for oral suspension, USP 200 mg/5 mL and erythromycin ethylsuccinate for oral suspension, USP 400 mg/5 mL must be stored at 20° to 25° C (68° to 77° F) and use…
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
D10AF02 Erythromycin
HS code (indicative)
3004.20Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
21 November 2022
Identifiers
RxCUI 686400, 686418DailyMed set ID 1d9eb7cb-0b11-4f6e-8a9c-1bcff37fe0b5, a7f7faaf-dc05-4d51-86c6-bf5d61562e48, db70798e-5e07-41d6-afe9-82c272bc5cc0NDC 72162-2657, 85742-029, 71209-102Application ANDA216212

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

Packs from every labeler of this generic presentation.

PackCodeLabelerMarketed since
100 mL in 1 bottle71209-102-21Cadila PharmaceuticalsIndia21 November 2022
100 mL in 1 bottle85742-029-28Kanchan Healthcare21 November 2022
100 mL in 1 bottle72162-2657-1Bryant Ranch Prepack5 June 2026

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 June 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

Other strengths and forms of Erythromycin

Clinical summary

Erythromycin is a macrolide antimicrobial indicated in the treatment of infections caused by susceptible strains of the designated organisms in the diseases listed below, among other approved uses. MedsAcross supplies Erythromycin 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 Erythromycin

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

Data sources

Need Erythromycin 200 mg/5 mL powder for oral suspension 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.