DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LEVLITE
FDA Application No:
(NDA) 020860
Active Ingredient(s):
ETHINYL ESTRADIOL; LEVONORGESTREL
Company:
BAYER HLTHC
Original Approval or Tentative Approval Date:
July 13, 1998
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
LEVLITE
ETHINYL ESTRADIOL; LEVONORGESTREL
0.02MG; 0.1MG
TABLET; ORAL-21
Discontinued
No
None
LEVLITE
ETHINYL ESTRADIOL; LEVONORGESTREL
0.02MG; 0.1MG
TABLET; ORAL-28
Prescription
Yes
AB2
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