DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ZEMURON
FDA Application No:
(NDA) 020214
Active Ingredient(s):
ROCURONIUM BROMIDE
Company:
ORGANON USA INC
Original Approval or Tentative Approval Date:
March 17, 1994
Chemical Type:
1 New molecular entity (NME)
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
ZEMURON
ROCURONIUM BROMIDE
50MG/5ML(10MG/ML)
INJECTABLE; INJECTION
Prescription
Yes
None
ZEMURON
ROCURONIUM BROMIDE
10MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
ZEMURON
ROCURONIUM BROMIDE
100MG/10ML(10MG/ML)
INJECTABLE; INJECTION
Prescription
Yes
None
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