DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FLOLAN
FDA Application No:
(NDA) 020444
Active Ingredient(s):
EPOPROSTENOL SODIUM
Company:
GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:
September 20, 1995
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
O Orphan 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
FLOLAN
EPOPROSTENOL SODIUM
EQ 0.5MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
None
FLOLAN
EPOPROSTENOL SODIUM
EQ 1.5MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
None
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