DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SINEMET
FDA Application No:
(NDA) 017555
Active Ingredient(s):
CARBIDOPA; LEVODOPA
Company:
BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date:
May 2, 1975
Chemical Type:
14 New molecular entity and new combination
Review Classification:
P Priority 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
SINEMET
CARBIDOPA; LEVODOPA
10MG; 100MG
TABLET; ORAL
Prescription
No
AB
SINEMET
CARBIDOPA; LEVODOPA
25MG; 250MG
TABLET; ORAL
Prescription
Yes
AB
SINEMET
CARBIDOPA; LEVODOPA
25MG; 100MG
TABLET; ORAL
Prescription
No
AB
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