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) 016979
Active Ingredient(s):
MEGESTROL ACETATE
Company:
BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date:
August 18, 1971
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MEGACE
MEGESTROL ACETATE
20MG
TABLET; ORAL
Prescription
No
AB
MEGACE
MEGESTROL ACETATE
40MG
TABLET; ORAL
Prescription
Yes
AB
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