DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ZOVIRAX
FDA Application No:
(NDA) 018603
Active Ingredient(s):
ACYCLOVIR SODIUM
Company:
GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:
October 22, 1982
Chemical Type:
23 New active ingredient and new dosage form
Review Classification:
P Priority review drug
Therapeutic Equivalents
Label Information
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
ZOVIRAX
ACYCLOVIR SODIUM
EQ 500MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
ZOVIRAX
ACYCLOVIR SODIUM
EQ 1GM BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
ZOVIRAX
ACYCLOVIR SODIUM
EQ 250MG BASE/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
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