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MedsAcross

Medicine

Nexplanon 68 mg implant

Etonogestrel · Subcutaneous · Organon
Available on requestPrescription onlyUS FDA

Nexplanon 68 mg implant is a prescription medicine containing Etonogestrel for subcutaneous use, marketed by Organon, 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 NEXPLANON at 20ºC to 25ºC (68ºF to 77ºF), excursions permitted between…

Key facts

Active ingredient (INN)
Etonogestrel
Brand
Nexplanon
Strength
68 mg
Dosage form
Implant
Route
Subcutaneous
Packs
1 blister pack
Marketing authorisation holder
Organon
Manufacturer
Organon
Origin register
US FDA, United States
Storage
Store NEXPLANON at 20ºC to 25ºC (68ºF to 77ºF), excursions permitted between 15ºC to 30ºC (59ºF to 86ºF). Avoid storing NEXPLANON at temperatures above 30ºC (86ºF).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
G03AC08 Etonogestrel
HS code (indicative)
3004.39Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
1 June 2021
Identifiers
RxCUI 389221, 1111011DailyMed set ID 487f8a62-e142-457c-97cc-2e398fde7594NDC 78206-145Application NDA021529

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
1 blister pack in 1 carton / 1 implant in 1 blister pack78206-145-01Organon1 June 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 17 July 2006Drugs@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

Etonogestrel is a progestin indicated for prevention of pregnancy in women of reproductive potential for up to 5 years. It is available as implants for subcutaneous use. MedsAcross supplies Etonogestrel 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 Etonogestrel

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

Data sources

Need Nexplanon 68 mg implant 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.