DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
OPHTHOCORT
FDA Application No:
(NDA) 050201
Active Ingredient(s):
CHLORAMPHENICOL; HYDROCORTISONE ACETATE; POLYMYXIN B SULFATE
Company:
PARKEDALE
Original Approval or Tentative Approval Date:
June 25, 1958
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
OPHTHOCORT
CHLORAMPHENICOL; HYDROCORTISONE ACETATE; POLYMYXIN B SULFATE
10MG/GM; 5MG/GM; 10,000 UNITS/GM
OINTMENT; OPHTHALMIC
Discontinued
No
None
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