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MedsAcross

Medicine

Cyproheptadine 2 mg/5 mL oral solution

Available on requestPrescription onlyUS FDAGeneric name

Cyproheptadine 2 mg/5 mL oral solution is a generic prescription medicine for oral use, made by 5 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 20°-25°C (68°-77°F) excursion permitted to 15°-30°C (59°-86°F).

Key facts

Active ingredient (INN)
Cyproheptadine
Brand
Sold under the generic name
Strength
2 mg/5 mL
Dosage form
Oral solution
Route
Oral
Packs
473 mL, 72 cup, 120 syringes and 5 more
Manufacturers
Atlantic BiologicalsBryant Ranch PrepackQuagen PharmaceuticalsMethod PharmaceuticalsPatrin Pharma
Origin register
US FDA, United States
Storage
Store at 20°-25°C (68°-77°F) excursion 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
R06AX02 Cyproheptadine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
22 May 2019
Identifiers
RxCUI 866021DailyMed set ID 582b86c6-f9b2-278d-e063-6394a90a923d, d3ce21de-849a-47ab-8405-968d8de6f1e9, 81d9523f-f945-4410-8b71-8b5fea48a3da +2NDC 17856-1185, 70752-185, 70752-101 +3Application ANDA212423, ANDA209108

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
473 mL in 1 bottle, glass70752-101-12Quagen Pharmaceuticals22 May 2019
473 mL in 1 bottle, plastic70752-185-12Quagen Pharmaceuticals22 December 2023
473 mL in 1 bottle, glass58657-697-16Method Pharmaceuticals15 June 2024
473 mL in 1 bottle, glass39328-544-16Patrin Pharma15 February 2022
72 cup, unit-dose in 1 case / 5 mL in 1 cup, unit-dose17856-1185-1Atlantic Biologicals4 August 2026
120 syringe in 1 case / 2.5 mL in 1 syringe17856-1185-2Atlantic Biologicals7 August 2026
473 mL in 1 bottle, glass72162-2065-2Bryant Ranch Prepack12 August 2024
473 mL in 1 bottle, glass72162-2065-4Bryant Ranch Prepack2 May 2025

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 17 October 1961Drugs@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 Cyproheptadine

Clinical summary

Cyproheptadine is a prescription medicine. It is available as tablets, oral solution and syrup. MedsAcross supplies Cyproheptadine 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 Cyproheptadine

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

Data sources

Need Cyproheptadine 2 mg/5 mL oral solution 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.