DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
TAMSULOSIN HYDROCHLORIDE
FDA Application No:
(ANDA) 078015
Active Ingredient(s):
TAMSULOSIN HYDROCHLORIDE
Company:
LEK PHARMS
Original Approval or Tentative Approval Date:
April 30, 2007
Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
TAMSULOSIN HYDROCHLORIDE
TAMSULOSIN HYDROCHLORIDE
0.4MG
CAPSULE; ORAL
Tentative Approval
No
None
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