DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ZITHROMAX
FDA Application No:
(NDA) 050784
Active Ingredient(s):
AZITHROMYCIN
Company:
PFIZER
Original Approval or Tentative Approval Date:
May 24, 2002
Chemical Type:
3 New dosage form
Review Classification:
S Standard 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
ZITHROMAX
AZITHROMYCIN
EQ 500MG BASE
TABLET; ORAL
Prescription
No
AB
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