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MedsAcross

Manufacturer

TerSera Therapeutics

Products listed
9
Molecules
6
Therapy areas
4

TerSera Therapeutics is a pharmaceutical manufacturer based in an unrecorded country. MedsAcross lists 9 of its products across 6 molecules, each with registers, packs and availability for export supply to licensed buyers.

Indian manufacturer
No
Also listed as
TerSera Therapeutics LLC
US FDA labeler
YesSource: openFDA NDC directory

Source from this manufacturer

We supply TerSera Therapeutics products through licensed channels, with the documents your regulator needs.

Pain and anaesthesia

3 presentations

Pain and anaesthesia overview
MedicineActive ingredientRegisterAvailability
Prialt 100 mcg/1 mL injectionIntrathecal Cold chainZiconotideUS FDAAvailable on request
Prialt 500 mcg/20 mL injectionIntrathecal Cold chainZiconotideUS FDAAvailable on request
Prialt 500 mcg/5 mL injectionIntrathecal Cold chainZiconotideUS FDAAvailable on request

Oncology

2 presentations

Oncology overview
MedicineActive ingredientRegisterAvailability
Zoladex 10.8 mg implantSubcutaneousGoserelinUS FDAAvailable on request
Zoladex 3.6 mg implantSubcutaneousGoserelinUS FDAAvailable on request

Gastroenterology

1 presentation

Gastroenterology overview
MedicineActive ingredientRegisterAvailability
Varubi 90 mg tabletOralRolapitantUS FDAAvailable on request

Rare diseases and enzyme replacement

1 presentation

Rare diseases and enzyme replacement overview
MedicineActive ingredientRegisterAvailability
Xermelo 250 mg tabletOralTelotristat ethylUS FDAAvailable on request

Other products

2 presentations

MedicineActive ingredientRegisterAvailability
Margenza 25 mg/mL injectionIntravenous Cold chainMargetuximabUS FDAAvailable on request
Quzyttir 10 mg/1 mL injectionIntravenousCetirizineUS FDAAvailable on request

Molecules made

Manufacturer facts come from public registers and are shown with their source. Listing does not mean the manufacturer endorses MedsAcross.

Source from TerSera Therapeutics

Send a request for any of these products. We confirm the licensed source, documents and lead time.