APO-Pregabalin

New Zealand - English - Medsafe (Medicines Safety Authority)

Active ingredient:
Pregabalin 50 mg
Available from:
Apotex NZ Ltd
INN (International Name):
Pregabalin 50 mg
Dosage:
50 mg
Pharmaceutical form:
Capsule
Composition:
Active: Pregabalin 50 mg Excipient: Gelatin   Lactose monohydrate Maize starch Purified talc Sodium laurilsulfate   Titanium dioxide   Water  
Prescription type:
Prescription
Manufactured by:
Srini Pharmaceuticals Pvt Ltd
Therapeutic indications:
Indicated for the treatment of neuropathic pain in adults.
Product summary:
Package - Contents - Shelf Life: Blister pack, PVC/Al - 14 capsules - 24 months from date of manufacture stored at or below 25°C - Blister pack, PVC/Al - 20 capsules - 24 months from date of manufacture stored at or below 25°C - Blister pack, PVC/Al - 56 capsules - 24 months from date of manufacture stored at or below 25°C - Blister pack, PVC/Al - 60 capsules - 24 months from date of manufacture stored at or below 25°C - Bottle, plastic, HDPE with child resistant PP cap - 14 capsules - 24 months from date of manufacture stored at or below 25°C - Bottle, plastic, HDPE with child resistant PP cap - 20 capsules - 24 months from date of manufacture stored at or below 25°C - Bottle, plastic, HDPE with child resistant PP cap - 56 capsules - 24 months from date of manufacture stored at or below 25°C - Bottle, plastic, HDPE with child resistant PP cap - 60 capsules - 24 months from date of manufacture stored at or below 25°C - Bottle, plastic, HDPE with PP cap - 100 capsules - 24 months from date of manufacture stored at or below 25°C - Bottle, plastic, HDPE with PP cap - 500 capsules - 24 months from date of manufacture stored at or below 25°C
Authorization number:
TT50-9471a
Authorization date:
2014-01-06

Similar products

Search alerts related to this product

Share this information