DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
HEMABATE
FDA Application No:
(NDA) 017989
Active Ingredient(s):
CARBOPROST TROMETHAMINE
Company:
PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date:
January 9, 1979
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
HEMABATE
CARBOPROST TROMETHAMINE
EQ 0.25MG BASE/ML
INJECTABLE; INJECTION
Prescription
Yes
None
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