DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
IBU-TAB 200
FDA Application No:
(ANDA) 071057
Active Ingredient(s):
IBUPROFEN
Company:
ALRA
Original Approval or Tentative Approval Date:
August 11, 1988
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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
IBU-TAB 200
IBUPROFEN
200MG
TABLET; ORAL
OTC
No
None
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