01 2ERYTHROMYCIN (ERYTHROMYCIN LACTOBIONATE)
02 1FUSIDIC ACID
03 1PILOCARPINE HYDROCHLORIDE
04 2PRUCALOPRIDE (PRUCALOPRIDE SUCCINATE)
01 1DROPS
02 2POWDER FOR SOLUTION
03 3TABLET
01 11%/W/W
02 11G/VIAL
03 11MG
04 12MG
05 1500MG/VIAL
06 15MG
01 2ERYTHROCIN I.V.
02 1FUCITHALMIC
03 2RESOTRAN
04 1SALAGEN
Regulatory Info : Prescription
Registration Country : Canada
Amdipharm Mercury Company Limited
Dosage Form : TABLET
Dosage Strength : 5MG
Packaging :
Brand Name : SALAGEN
Approval Date :
Application Number : 2216345
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
ERYTHROMYCIN (ERYTHROMYCIN LACTOBIONATE)
Amdipharm Mercury Company Limited
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500MG/VIAL
Packaging : 10ML
Brand Name : ERYTHROCIN I.V.
Approval Date :
Application Number : 682268
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
ERYTHROMYCIN (ERYTHROMYCIN LACTOBIONATE)
Amdipharm Mercury Company Limited
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1G/VIAL
Packaging : 20ML
Brand Name : ERYTHROCIN I.V.
Approval Date :
Application Number : 682276
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Amdipharm Mercury Company Limited
Dosage Form : DROPS
Dosage Strength : 1%/W/W
Packaging : 5G
Brand Name : FUCITHALMIC
Approval Date :
Application Number : 2243862
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
PRUCALOPRIDE (PRUCALOPRIDE SUCCINATE)
Amdipharm Mercury Company Limited
Dosage Form : TABLET
Dosage Strength : 1MG
Packaging : 28
Brand Name : RESOTRAN
Approval Date :
Application Number : 2377012
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
PRUCALOPRIDE (PRUCALOPRIDE SUCCINATE)
Amdipharm Mercury Company Limited
Dosage Form : TABLET
Dosage Strength : 2MG
Packaging : 28
Brand Name : RESOTRAN
Approval Date :
Application Number : 2377020
Regulatory Info : Prescription
Registration Country : Canada
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