DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ACETAMINOPHEN AND HYDROCODONE BITARTRATE
FDA Application No:
(ANDA) 088898
Active Ingredient(s):
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Company:
CENT PHARMS
Original Approval or Tentative Approval Date:
March 27, 1985
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
ACETAMINOPHEN AND HYDROCODONE BITARTRATE
ACETAMINOPHEN; HYDROCODONE BITARTRATE
500MG; 5MG
CAPSULE; ORAL
Discontinued
No
None
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