DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NAFCILLIN SODIUM
FDA Application No:
(ANDA) 062732
Active Ingredient(s):
NAFCILLIN SODIUM
Company:
SANDOZ
Original Approval or Tentative Approval Date:
December 23, 1986
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
NAFCILLIN SODIUM
NAFCILLIN SODIUM
EQ 1GM BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
NAFCILLIN SODIUM
NAFCILLIN SODIUM
EQ 2GM BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
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