DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
KANAMYCIN
FDA Application No:
(ANDA) 065111
Active Ingredient(s):
KANAMYCIN SULFATE
Company:
ABRAXIS PHARM
Original Approval or Tentative Approval Date:
December 17, 2002
Therapeutic Equivalents
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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
KANAMYCIN
KANAMYCIN SULFATE
EQ 500MG BASE/2ML
INJECTABLE; INJECTION
Prescription
No
AP
KANAMYCIN
KANAMYCIN SULFATE
EQ 1GM BASE/3ML
INJECTABLE; INJECTION
Prescription
No
AP
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