DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
REMODULIN
FDA Application No:
(NDA) 021272
Active Ingredient(s):
TREPROSTINIL SODIUM
Company:
UNITED THERAP
Original Approval or Tentative Approval Date:
May 21, 2002
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
REMODULIN
TREPROSTINIL SODIUM
1MG/ML
INJECTABLE; IV (INFUSION)-SC
Prescription
No
None
REMODULIN
TREPROSTINIL SODIUM
2.5MG/ML
INJECTABLE; IV (INFUSION)-SC
Prescription
No
None
REMODULIN
TREPROSTINIL SODIUM
5MG/ML
INJECTABLE; IV (INFUSION)-SC
Prescription
No
None
REMODULIN
TREPROSTINIL SODIUM
10MG/ML
INJECTABLE; IV (INFUSION)-SC
Prescription
Yes
None
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