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Chloromycetin HydrocortisoneDrug - Chloromycetin Hydrocortisone The trade name of the product as shown on the labeling.
Dosage -
FOR SUSPENSION; OPHTHALMIC
Active Ingredient(s) -
Chloramphenicol; Hydrocortisone Acetate
Strength -
12.5MG/VIAL;25MG/VIAL
Applicant -
PARKEDALE
New Drug Application (NDA) Number -
050202
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Parkedale Pharmaceuticals Inc
Chloromycetin Hydrocortisone
Chloromycetin Hydrocortisone 12.5mg/vial;25mg/vial For Suspension; Ophthalmic
Chloromycetin 0.5% Solution/drops; Otic Chloromycetin Palmitate Eq 150mg Base/5ml Suspension; Oral Chloromycetin Palmitate Eq 150mg Base/5ml Suspension; Oral Chloramphenicol Eq 1gm Base/vial Injectable; Injection Chloramphenicol Sodium Succinate Eq 1gm Base/vial Injectable; Injection Chloramphenicol Sodium Succinate Eq 1gm Base/vial Injectable; Injection Chloromycetin Eq 1gm Base/vial Injectable; Injection Mychel-s Eq 1gm Base/vial Injectable; Injection Elase-chloromycetin 10mg/gm;666 Units/gm;1 Units/gm Ointment; Topical NewDrugInformation |