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ZofranDrug - Zofran The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Ondansetron Hydrochloride
Strength -
EQ 4MG BASE
Applicant -
GLAXOSMITHKLINE
New Drug Application (NDA) Number -
020103
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Dec 31, 1992
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Glaxosmithkline
Zofran
Zofran Eq 4mg Base/5ml Solution; Oral
Zofran Eq 24mg Base Tablet; Oral Zofran Eq 4mg Base Tablet; Oral Zegerid 40mg/packet For Suspension; Oral Prilosec Otc Eq 20mg Base Tablet, Delayed Release; Oral Zofran Odt Eq 4mg Base Tablet, Orally Disintegrating; Oral Zofran Odt Eq 8mg Base Tablet, Orally Disintegrating; Oral Zofran Eq 2mg Base/ml Injectable; Injection Zofran In Plastic Container Eq 0.64mg Base/ml Injectable; Injection Zofran Preservative Free Eq 2mg Base/ml Injectable; Injection NewDrugInformation |