DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SOTRET
FDA Application No:
(ANDA) 076503
Active Ingredient(s):
ISOTRETINOIN
Company:
RANBAXY
Original Approval or Tentative Approval Date:
June 20, 2003
Therapeutic Equivalents
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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
SOTRET
ISOTRETINOIN
30MG
CAPSULE; ORAL
Prescription
No
AB
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