DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
BETAXOLOL
FDA Application No:
(ANDA) 075386
Active Ingredient(s):
BETAXOLOL HYDROCHLORIDE
Company:
AKORN
Original Approval or Tentative Approval Date:
June 30, 2000
Therapeutic Equivalents
Labels are not available
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
BETAXOLOL
BETAXOLOL HYDROCHLORIDE
EQ 0.5% BASE
SOLUTION/DROPS; OPHTHALMIC
Prescription
No
AT
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