DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
RETIN-A
FDA Application No:
(NDA) 017522
Active Ingredient(s):
TRETINOIN
Company:
JOHNSON AND JOHNSON
Original Approval or Tentative Approval Date:
July 19, 1974
Chemical Type:
5 New manufacturer
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
RETIN-A
TRETINOIN
0.05%
CREAM; TOPICAL
Prescription
Yes
AB1
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