DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CHILDREN'S ADVIL
FDA Application No:
(NDA) 020589
Active Ingredient(s):
IBUPROFEN
Company:
WYETH CONS
Original Approval or Tentative Approval Date:
June 27, 1996
Chemical Type:
8 OTC (over-the-counter) switch
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
CHILDREN'S ADVIL
IBUPROFEN
100MG/5ML
SUSPENSION; ORAL
OTC
No
None
CHILDREN'S ADVIL-FLAVORED
IBUPROFEN
100MG/5ML
SUSPENSION; ORAL
OTC
No
None
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