DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SODIUM CHLORIDE 3% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 019635
Active Ingredient(s):
SODIUM CHLORIDE
Company:
B BRAUN
Original Approval or Tentative Approval Date:
March 9, 1988
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
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
SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
SODIUM CHLORIDE
450MG/100ML
INJECTABLE; INJECTION
Prescription
No
AP
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
SODIUM CHLORIDE
900MG/100ML
INJECTABLE; INJECTION
Prescription
Yes
AP
SODIUM CHLORIDE 3% IN PLASTIC CONTAINER
SODIUM CHLORIDE
3GM/100ML
INJECTABLE; INJECTION
Discontinued
No
None
SODIUM CHLORIDE 5% IN PLASTIC CONTAINER
SODIUM CHLORIDE
5GM/100ML
INJECTABLE; INJECTION
Discontinued
No
None
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