DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MEGACE
FDA Application No:
(NDA) 020264
Active Ingredient(s):
MEGESTROL ACETATE
Company:
BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date:
September 10, 1993
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
O Orphan drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MEGACE
MEGESTROL ACETATE
40MG/ML
SUSPENSION; ORAL
Prescription
Yes
AB
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