DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PROMETHACON
FDA Application No:
(ANDA) 084902
Active Ingredient(s):
PROMETHAZINE HYDROCHLORIDE
Company:
POLYMEDICA
Original Approval or Tentative Approval Date:
October 5, 1981
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
PROMETHACON
PROMETHAZINE HYDROCHLORIDE
50MG
SUPPOSITORY; RECTAL
Discontinued
No
None
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