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Ocrelizumab

BATCH NUMBER: H0037B29

515,00 

Therapeutic Ocrelizumab antibody from the original Ocrevus® commercial drug

In stock

Certificate of Analysis (CoA) is an official document issued by the manufacturer of the medicinal product. It contains information on some critical quality characteristics of the medicine.

Product specifications:​

  • Product Concentration 30 mg/mL
  • Volume per vial 100 µL
  • Quantity per vial 3 mg
  • Batch Number H0037B29
  • Storage Temperature -80°C
Our products are for research use only. The “therapeutic expiration date” implies expiry date for patient adminstration and is not applicable to the shelf life of the aliquot. Aliquot storage at -86°C ensures fully functional molecules even after the mentioned expiry date

Product Information:

Evidentic offers repackaged finished pharmaceutical products (e.g RMP/RLD). We refer to the repackaged RMP/RLD products synonymously as drug aliquots or aRMP, or short: aliquots.

We offer batches of original drug aliquots in low-binding Eppendorf tubes for research use only. We provide license-free drug aliquots with long, short or even “negative shelf life” by storing the products at recommended temperatures (either 2-8°C or -80°C) and ensuring fully functional molecules for research purposes.

As ‘raw material’ for the production of drug aliquots, Evidentic sources RMP from the European (EU) market. As a licensed pharmaceutical wholesaler, Evidentic is committed to Good Distribution Practice (GDP) compliance with respect to the procurement, storage and shipment of RMP.
Drug aliquots are manufactured by repackaging RMP in a qualified laboratory. The aliquotation process is performed under a quality and manufacturing agreement between Evidentic and the contract manufacturer. Repackaging of RMP includes the following steps: opening the secondary and primary RMP containers and transferring the specified volumes of RMP into an Eppendorf 0.5 ml low-binding (or similar) tube. If the RMP is a lyophilized powder and not a highly concentrated solution, reconstitute the RMP according to the original manufacturer’s instructions and then aliquot as a highly concentrated solution.
For identification purposes, drug aliquots are labeled with the date of aliquoting, the original lot number of the RMP, the original expiration date of the RMP, the name of the active ingredient (INN), and a unique identification code.
Immediately after aliquoting, drug aliquots are stored at either 2-8 °C or -86 °C for long-term storage. All drug aliquots stored at 2-8 °C are transferred to -86 °C at least two weeks before the expiration date of the original RLD/RMP is reached. Further quality or functional testing are not performed on the drug aliquots.  

Class of molecule

Host cells

Chinese Hamster Ovary (CHO) cells

Prepared from (Reference drug)​

Ocrevus(R)®

Therapeutic Area

Therapeutic Indications

Mechanism of Action (MoA)

Presumed to involve immunomodulation through the reduction in the number and function of CD20-expressing B cells

Pharmacotherapeutic group​​

Selective immunosuppressants group

List of Excipients​

Sodium Acetate Trihydrate
Glacial Acetic Acid
Trehalose Dihydrate
Polysorbate 20

More Reference Drugs as Aliquots

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CD20
Monoclonal Antibody
Ocrevus®
30 mg/mL
100 µL
3 mg
2-8°C / -80°C
09/2021
515,00 
view product
Max: 54
Min: 1
Step: 1
CD20
Monoclonal Antibody
Ocrevus®
30 mg/mL
100 µL
3 mg
2-8°C / -80°C
09/2021
515,00 
view product
Max: 55
Min: 1
Step: 1
CD20
Monoclonal Antibody
Ocrevus®
30 mg/mL
100 µL
3 mg
2-8°C / -80°C
09/2021
515,00 
view product
Max: 55
Min: 1
Step: 1

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