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) 077787
Active Ingredient(s):
METFORMIN HYDROCHLORIDE
Company:
DR REDDYS LABS INC
Original Approval or Tentative Approval Date:
August 23, 2006
Therapeutic Equivalents
Labels are not available
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
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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