DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NEO-DELTA-CORTEF
FDA Application No:
(ANDA) 061037
Active Ingredient(s):
NEOMYCIN SULFATE; PREDNISOLONE ACETATE
Company:
PHARMACIA AND UPJOHN
There are no Therapeutic Equivalents
Labels are not available
Approval History and Related Documents are not available
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
NEO-DELTA-CORTEF
NEOMYCIN SULFATE; PREDNISOLONE ACETATE
EQ 3.5MG BASE/ML; 0.25%
SUSPENSION/DROPS; OPHTHALMIC
Discontinued
No
None
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