DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
TERBINAFINE HYDROCHLORIDE
FDA Application No:
(ANDA) 076377
Active Ingredient(s):
TERBINAFINE HYDROCHLORIDE
Company:
TEVA
Original Approval or Tentative Approval Date:
July 2, 2007
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
TERBINAFINE HYDROCHLORIDE
TERBINAFINE HYDROCHLORIDE
EQ 250MG BASE
TABLET; ORAL
Prescription
No
AB
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