DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DIETHYLPROPION HYDROCHLORIDE
FDA Application No:
(ANDA) 088268
Active Ingredient(s):
DIETHYLPROPION HYDROCHLORIDE
Company:
TG UNITED LABS
Original Approval or Tentative Approval Date:
August 25, 1983
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
DIETHYLPROPION HYDROCHLORIDE
DIETHYLPROPION HYDROCHLORIDE
25MG
TABLET; ORAL
Discontinued
No
None
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