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Medicine

Pertzye 90750 units/24000 units/86250 units delayed-release capsule

Available on requestPrescription onlyUS FDA

Pertzye 90750 units/24000 units/86250 units delayed-release capsule is a prescription medicine containing Pancrelipase amylase, Pancrelipase lipase and Pancrelipase protease for oral use, marketed by Digestive Care, 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 PERTZYE at room temperature 20°C to 25°C (68°F to 77°F), excursions…

Key facts

Active ingredient (INN)
Pancrelipase amylase, Pancrelipase lipase and Pancrelipase protease
Brand
Pertzye
Strength
90750 units/24000 units/86250 units
Dosage form
Delayed-release capsule
Route
Oral
Packs
80 capsules, 200 capsules
Marketing authorisation holder
Digestive Care
Manufacturer
Digestive Care
Origin register
US FDA, United States
Storage
Store PERTZYE at room temperature 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 40°C (59°F to 104°F) for up to 30 days. PERTZYE hard gelatin capsules should be stored in a dry place in the original container or equivalent airtight container. After opening, keep the container tightly closed between uses to protect from moisture.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
HS code (indicative)
3002.15Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
13 July 2017
Identifiers
RxCUI 1294122, 1294128, 1294481 +5DailyMed set ID 481eec00-9abf-11dd-b71c-0002a5d5c51bNDC 59767-024Application BLA022175

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
80 capsule, delayed release in 1 bottle59767-024-01Digestive Care13 July 2017
200 capsule, delayed release in 1 bottle59767-024-02Digestive Care13 July 2017

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
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 Pancrelipase amylase, Pancrelipase lipase and Pancrelipase protease

Clinical summary

Pancrelipase amylase, Pancrelipase lipase and Pancrelipase protease is a fixed-dose combination medicine indicated for the treatment of exocrine pancreatic insufficiency in adult and pediatric patients. MedsAcross supplies Pancrelipase amylase, Pancrelipase lipase and Pancrelipase protease 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 Pancrelipase amylase, Pancrelipase lipase and Pancrelipase protease

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

Data sources

Need Pertzye 90750 units/24000 units/86250 units delayed-release 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.