Active Ingredient: METRONIDAZOLE HYDROCHLORIDE
Proprietary Name: METRONIDAZOLE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070295
Product Number: 001
Approval Date: Oct 15, 1985
Applicant Holder Full Name: ABRAXIS PHARMACEUTICAL PRODUCTS
Marketing Status:
Discontinued
Patent and Exclusivity Information
