TGA Approval

AMCAL+ IBUPROFEN SODIUM DIHYDRATE 256 MG film coated tablet blister pack (443150)

ARTG ID

443150

ARTG Name

AMCAL+ IBUPROFEN SODIUM DIHYDRATE 256 MG film coated tablet blister pack

Sponsor

Neo Health (OTC) Pty Ltd

ARTG Date

March 4, 2024

Registration Type

Medicine

Therapeutic Good Type

Medicine

Licence Status

Active

Licence Category

Registered

Sponsor Information

Sponsor Name

Sponsor Item Name

NEO HEALTH (OTC) PTY LTD

Ingredient Name

ibuprofen sodium dihydrate

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AMCAL+ IBUPROFEN SODIUM DIHYDRATE 256 MG film coated tablet blister pack (443150) - TGA 批准文号 | MedPath