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Medicine

Penicillamine 250 mg capsule

Available on requestPrescription onlyUS FDAGeneric name

Penicillamine 250 mg capsule is a generic prescription medicine for oral use, made by 7 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 o to 25 • C (68 o to 77 • F).

Key facts

Active ingredient (INN)
Penicillamine
Brand
Sold under the generic name
Strength
250 mg
Dosage form
Capsule
Route
Oral
Packs
100 capsules and 4 more
Manufacturers
Dr. Reddy's LaboratoriesIndiaGranules IndiaIndiaActavis PharmaBreckenridge PharmaceuticalNavintaPar HealthProficient Rx
Origin register
US FDA, United States
Storage
Store at 20 o to 25 • C (68 o to 77 • F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
M01CC01 Penicillamine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
25 June 2019
Identifiers
RxCUI 198070DailyMed set ID f658b20a-269f-4e78-a79b-a56a5ed8dc1b, 594d7a82-af1d-41c4-98ee-0ea6895fc237, 01e79d8f-8c74-4f48-b761-9f225fabf93d +4NDC 70010-907, 0591-4171, 49884-146 +4Application ANDA211735, ANDA210976, ANDA211231 +3

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 capsule, gelatin coated in 1 bottle43598-634-01Dr. Reddy's LaboratoriesIndia4 August 2020
100 capsule in 1 bottle70010-907-01Granules IndiaIndia21 December 2020
100 capsule in 1 bottle0591-4171-01Actavis Pharma25 June 2019
100 capsule in 1 bottle51991-974-01Breckenridge Pharmaceutical12 November 2021
100 capsule in 1 bottle68475-201-01Navinta1 January 2022
100 capsule in 1 bottle49884-146-01Par Health8 January 2020
100 capsule in 1 bottle71205-916-00Proficient Rx8 July 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 4 December 1970Drugs@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

Alternatives

Other makers and brands of Penicillamine 250 mg capsule.

Compare all 2

Other strengths and forms of Penicillamine

Clinical summary

Penicillamine is an antirheumatic agent indicated in the treatment of Wilson’s disease, cystinuria, and in patients with severe, active rheumatoid arthritis who have failed to respond to an adequate trial of conventional therapy. MedsAcross supplies Penicillamine 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 Penicillamine

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

Data sources

Need Penicillamine 250 mg capsule 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.