DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
FDA Application No:
(ANDA) 065216
Active Ingredient(s):
HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Company:
PHARMAFORCE
Original Approval or Tentative Approval Date:
October 31, 2005
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
1%; EQ 3.5MG BASE/ML; 10,000 UNITS/ML
SOLUTION/DROPS; OTIC
Prescription
No
AT
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