DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ULTANE
FDA Application No:
(NDA) 020478
Active Ingredient(s):
SEVOFLURANE
Company:
ABBOTT
Original Approval or Tentative Approval Date:
June 7, 1995
Chemical Type:
1 New molecular entity (NME)
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
ULTANE
SEVOFLURANE
100%
LIQUID; INHALATION
Prescription
Yes
AN
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