DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GALANTAMINE HYDROBROMIDE
FDA Application No:
(ANDA) 077585
Active Ingredient(s):
GALANTAMINE HYDROBROMIDE
Company:
ACTAVIS ELIZABETH
Original Approval or Tentative Approval Date:
April 17, 2007
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
GALANTAMINE HYDROBROMIDE
GALANTAMINE HYDROBROMIDE
EQ 4MG BASE
TABLET; ORAL
Tentative Approval
No
None
GALANTAMINE HYDROBROMIDE
GALANTAMINE HYDROBROMIDE
EQ 8MG BASE
TABLET; ORAL
Tentative Approval
No
None
GALANTAMINE HYDROBROMIDE
GALANTAMINE HYDROBROMIDE
EQ 12MG BASE
TABLET; ORAL
Tentative Approval
No
None
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