DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GENCEPT 10/11-21
FDA Application No:
(ANDA) 072694
Active Ingredient(s):
ETHINYL ESTRADIOL; NORETHINDRONE
Company:
BARR
Original Approval or Tentative Approval Date:
February 28, 1992
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
GENCEPT 10/11-21
ETHINYL ESTRADIOL; NORETHINDRONE
0.035MG,0.035MG; 0.5MG,1MG
TABLET; ORAL-21
Prescription
No
AB
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