DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PASKALIUM
FDA Application No:
(NDA) 009395
Active Ingredient(s):
POTASSIUM AMINOSALICYLATE
Company:
GLENWOOD
Original Approval or Tentative Approval Date:
November 18, 1955
Chemical Type:
2 New active ingredient
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
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
PASKALIUM
POTASSIUM AMINOSALICYLATE
1GM
TABLET; ORAL
Discontinued
No
None
PASKALIUM
POTASSIUM AMINOSALICYLATE
500MG
CAPSULE; ORAL
Discontinued
No
None
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