DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GRISACTIN ULTRA
FDA Application No:
(ANDA) 062178
Active Ingredient(s):
GRISEOFULVIN, ULTRAMICROCRYSTALLINE
Company:
WYETH AYERST
Original Approval or Tentative Approval Date:
March 13, 1980
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
GRISACTIN ULTRA
GRISEOFULVIN, ULTRAMICROCRYSTALLINE
125MG
TABLET; ORAL
Discontinued
No
None
GRISACTIN ULTRA
GRISEOFULVIN, ULTRAMICROCRYSTALLINE
250MG
TABLET; ORAL
Discontinued
No
None
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