Active Ingredient: OLANZAPINE
Proprietary Name: ZYPREXA
Dosage Form; Route of Administration: POWDER; INTRAMUSCULAR
Strength: 10MG/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N021253
Product Number: 001
Approval Date: Mar 29, 2004
Applicant Holder Full Name: CHEPLAPHARM REGISTRATION GMBH
Marketing Status:
Prescription
Patent and Exclusivity Information
