DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
VANCOCIN HYDROCHLORIDE
FDA Application No:
(ANDA) 062716
Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE
Company:
VIROPHARMA
Original Approval or Tentative Approval Date:
March 13, 1987
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
VANCOCIN HYDROCHLORIDE
VANCOMYCIN HYDROCHLORIDE
EQ 500MG BASE/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
VANCOCIN HYDROCHLORIDE
VANCOMYCIN HYDROCHLORIDE
EQ 1GM BASE/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
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