Registered Uganda · NDA

LIVE ATTENUATED BOVINE HUMAN ROTAVIRUS REASSORTANT [G1, G2, G3, G4 AND G9]

Q: Is LIVE ATTENUATED BOVINE - HUMAN ROTAVIRUS REASSORTANT [G1, G2, G3, G4 AND G9] registered in Uganda?

LIVE ATTENUATED BOVINE - HUMAN ROTAVIRUS REASSORTANT [G1, G2, G3, G4 AND G9] is recorded with registration status “Registered” in Uganda, registration number NDA/MAL/HDP/10050, based on NDA data.

Q: Who manufactures LIVE ATTENUATED BOVINE - HUMAN ROTAVIRUS REASSORTANT [G1, G2, G3, G4 AND G9]?

LIVE ATTENUATED BOVINE - HUMAN ROTAVIRUS REASSORTANT [G1, G2, G3, G4 AND G9] is manufactured by Serum Institute Of India Pvt Ltd.

NDA/MAL/HDP/10050 PARENTERAL ORDINARY VIALS ?105.6 FFU / SEROTYPE PER DOSE (2 ML)

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Registration & product details

Registration no.

NDA/MAL/HDP/10050

Registration date

19/07/2022

Expiry date

Status

Registered

Active ingredient

Dosage form

PARENTERAL ORDINARY VIALS

Strength

?105.6 FFU / SEROTYPE PER DOSE (2 ML)

Pack size

1.0X2.0 ML VIAL, 1.0X50.0X2.0 ML VIAL

Therapeutic class

Manufacturer / MAH

Serum Institute Of India Pvt Ltd

Applicant / LTR

SERUM INSTITUTE OF INDIA PVT LTD

Country of origin

INDIA

Manufacturer location

Serum Institute Of India, 212/2, off Soli Poonawalla Road, Parijat Colony, Sadhana Society, Hadapsar, Pune, Maharashtra 411028, India

Source: National Drug Authority · fetched 2026-04-21 17:37:05 · updated 2026-09-12 04:00:19

Disclaimer: This information is sourced from National Drug Authority (Uganda). Always consult a qualified healthcare professional before using any medication.