DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ULTRAM
FDA Application No:
(NDA) 020281
Active Ingredient(s):
TRAMADOL HYDROCHLORIDE
Company:
ORTHO MCNEIL PHARM
Original Approval or Tentative Approval Date:
March 3, 1995
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
There are no 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
ULTRAM
TRAMADOL HYDROCHLORIDE
100MG
TABLET; ORAL
Discontinued
No
None
ULTRAM
TRAMADOL HYDROCHLORIDE
50MG
TABLET; ORAL
Prescription
Yes
AB
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