Baxter

Biosimilar developer, United States. 3 development products across 2 molecules: enoxaparin sodium, insulin human.

First approval in the Atlas: Aug 2022, Myxredlin, insulin human (HC)
FDAproducts approved0
EMAproducts approved0
MHRAproducts approved0
PMDAproducts approved0
HCproducts approved2
CDSCOproducts approved0
EDEproducts registered0

About Baxter

Baxter, the hospital products company, has two products that count as biosimilars only in Canada: Myxredlin, a ready-to-use intravenous human insulin, and Axberi, an enoxaparin. Myxredlin was approved as a drug in the United States and withdrawn in Europe without launch under the name Inpremzia.

Portfolio by market

MoleculeProductFDAEMAMHRAPMDAHCCDSCOEDEMarkets
Enoxaparin sodiumAxberi····Jul 2023··1/7
Insulin humanInpremzia·withdrawn·····0/7
Insulin humanMyxredlin····Aug 2022··1/7

Month shown is the first approval or registration of that product in that market.

Companies on the same molecules

Developers whose portfolios overlap most with Baxter, by number of shared molecules. Overlap is the clearest sign of who competes with whom for the same tenders and licensing partners.

Chronology

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Data current to September 2026.