DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(ANDA) 062414
Active Ingredient(s):
GENTAMICIN SULFATE
Company:
HOSPIRA
Original Approval or Tentative Approval Date:
August 15, 1983
Therapeutic Equivalents
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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
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 1.2MG BASE/ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 1.4MG BASE/ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 1.6MG BASE/ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 1.8MG BASE/ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 2MG BASE/ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 60MG BASE/100ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 70MG BASE/100ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 80MG BASE/100ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 90MG BASE/100ML
INJECTABLE; INJECTION
Prescription
No
AP
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
GENTAMICIN SULFATE
EQ 100MG BASE/100ML
INJECTABLE; INJECTION
Prescription
No
AP
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