DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
IBUPROFEN
FDA Application No:
(ANDA) 071639
Active Ingredient(s):
IBUPROFEN
Company:
VINTAGE PHARMS
Original Approval or Tentative Approval Date:
February 2, 1988
Therapeutic Equivalents
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You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
IBUPROFEN
IBUPROFEN
200MG
TABLET; ORAL
OTC
No
None
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