DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
WYAMINE SULFATE
FDA Application No:
(NDA) 008248
Active Ingredient(s):
MEPHENTERMINE SULFATE
Company:
BAXTER HLTHCARE CORP
Original Approval or Tentative Approval Date:
December 29, 1951
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
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
WYAMINE SULFATE
MEPHENTERMINE SULFATE
EQ 30MG BASE/ML
INJECTABLE; INJECTION
Discontinued
No
None
WYAMINE SULFATE
MEPHENTERMINE SULFATE
EQ 15MG BASE/ML
INJECTABLE; INJECTION
Discontinued
No
None
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