DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
METFORMIN HYDROCHLORIDE
FDA Application No:
(ANDA) 076033
Active Ingredient(s):
METFORMIN HYDROCHLORIDE
Company:
ACTAVIS ELIZABETH
Original Approval or Tentative Approval Date:
January 24, 2002
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
METFORMIN HYDROCHLORIDE
METFORMIN HYDROCHLORIDE
500MG
TABLET; ORAL
Prescription
No
AB
METFORMIN HYDROCHLORIDE
METFORMIN HYDROCHLORIDE
850MG
TABLET; ORAL
Prescription
No
AB
METFORMIN HYDROCHLORIDE
METFORMIN HYDROCHLORIDE
1GM
TABLET; ORAL
Prescription
No
AB
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