DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
METHOTREXATE PRESERVATIVE FREE
FDA Application No:
(NDA) 040265
Active Ingredient(s):
METHOTREXATE SODIUM
Company:
ABRAXIS PHARM
Original Approval or Tentative Approval Date:
February 26, 1999
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
METHOTREXATE PRESERVATIVE FREE
METHOTREXATE SODIUM
EQ 25MG BASE/ML
INJECTABLE; INJECTION
Discontinued
No
None
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