Efexor

New Zealand - English - Medsafe (Medicines Safety Authority)

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Active ingredient:
Venlafaxine hydrochloride 56.5 mg equivalent to 50 mg venlafaxine base;  
Available from:
Wyeth (NZ) Ltd
INN (International Name):
Venlafaxine hydrochloride 56.5 mg (equivalent to 50 mg venlafaxine base)
Dosage:
50 mg
Pharmaceutical form:
Tablet
Composition:
Active: Venlafaxine hydrochloride 56.5 mg equivalent to 50 mg venlafaxine base   Excipient: Ferrous oxide Iron oxide yellow Lactose monohydrate Magnesium stearate Microcrystalline cellulose Sodium starch glycolate
Units in package:
Blister pack, PVC or ACLAR or PVdC 1x30, 30 tablets
Class:
Prescription
Prescription type:
Prescription
Manufactured by:
ZaCh System, S.A.
Product summary:
Package - Contents - Shelf Life: Blister pack, PVC or ACLAR or PVdC 1x30 - 30 tablets - 36 months from date of manufacture stored at or below 30°C - Blister pack, PVC or ACLAR or PVdC 1x56 - 56 tablets - 36 months from date of manufacture stored at or below 30°C - Blister pack, PVC or ACLAR or PVdC 1x60 - 60 tablets - 36 months from date of manufacture stored at or below 30°C - Blister pack, PVC or ACLAR or PVdC 1x90 - 90 tablets - 36 months from date of manufacture stored at or below 30°C - Bottle, plastic, 1x30 - 30 tablets - 36 months from date of manufacture stored at or below 30°C - Bottle, plastic, 1x56 - 56 tablets - 36 months from date of manufacture stored at or below 30°C - Bottle, plastic, 1x60 - 60 tablets - 36 months from date of manufacture stored at or below 30°C - Bottle, plastic, 1x90 - 90 tablets - 36 months from date of manufacture stored at or below 30°C
Authorization number:
TT50-4638/1c
Authorization date:
1992-03-03

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