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HSA Approval

BANEOCIN POWDER

Approval Number

SIN00678P

Drug Name

BANEOCIN POWDER

Product Name

BANEOCIN POWDER

Approval Date

May 3, 1988

Registrant

NOVARTIS (SINGAPORE) PTE LTD

Licence Holder

SANDOZ SINGAPORE PTE. LTD.

Regulatory Information

Registrant

NOVARTIS (SINGAPORE) PTE LTD

Licence Holder

SANDOZ SINGAPORE PTE. LTD.

Drug Type

Therapeutic

Forensic Classification

Prescription Only

Formulation Information

Dosage Form

POWDER

Route of Administration

TOPICAL

Medical Information

ATC Code

D06AX04

ATC Item Name

neomycin

Manufacturer Information

Pharmaceutical Manufacturer

SANDOZ SINGAPORE PTE. LTD.

Manufacturers

PHARMAZEUTISCHE FABRIK MONTAVIT GMBH

Active Ingredients

Ingredient Name

BACITRACIN ZINC

Strength

250 iu/g

Drug MonographBacitracin

Ingredient Name

NEOMYCIN SULPHATE EQV NEOMYCIN

Strength

5000 iu/g

Drug MonographNeomycin

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