Active Ingredient: CHLORAMPHENICOL SODIUM SUCCINATE
Proprietary Name: CHLOROMYCETIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N050155
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKEDALE PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information