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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 012382

LARGON (PROPIOMAZINE HYDROCHLORIDE)
20MG/ML
Marketing Status: Discontinued
Active Ingredient: PROPIOMAZINE HYDROCHLORIDE
Proprietary Name: LARGON
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N012382
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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