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Chloramphenicol Sodium SuccinateDrug - Chloramphenicol Sodium Succinate The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Chloramphenicol Sodium Succinate
Strength -
EQ 1GM BASE/VIAL
Applicant -
AM PHARM PARTNERS
New Drug Application (NDA) Number -
062365
Product Number -
001
Therapeutic Equivalence (TE) Code -
AP
Approval Date -
Aug 25, 1982
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
American Pharmaceutical Partners Inc
Chloramphenicol Sodium Succinate
Optomycin 0.5% Solution/drops; 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 Chlorofair 0.5% Solution/drops; Ophthalmic Chloroptic 0.5% Solution/drops; Ophthalmic Econochlor 0.5% Solution/drops; Ophthalmic Ophthochlor 0.5% Solution/drops; Ophthalmic NewDrugInformation |