DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NEBCIN
FDA Application No:
(ANDA) 062008
Active Ingredient(s):
TOBRAMYCIN SULFATE
Company:
LILLY
Original Approval or Tentative Approval Date:
October 1, 1976
There are no 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
NEBCIN
TOBRAMYCIN SULFATE
EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
INJECTABLE; INJECTION
Discontinued
No
None
NEBCIN
TOBRAMYCIN SULFATE
EQ 10MG BASE/ML
INJECTABLE; INJECTION
Discontinued
No
None
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