DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NEOPAP
FDA Application No:
(NDA) 016401
Active Ingredient(s):
ACETAMINOPHEN
Company:
POLYMEDICA
Original Approval or Tentative Approval Date:
November 7, 1968
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
NEOPAP
ACETAMINOPHEN
120MG
SUPPOSITORY; RECTAL
OTC
No
None
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