DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CALCIBIND
FDA Application No:
(NDA) 018757
Active Ingredient(s):
CELLULOSE SODIUM PHOSPHATE
Company:
MISSION PHARMA
Original Approval or Tentative Approval Date:
December 28, 1982
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority 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
CALCIBIND
CELLULOSE SODIUM PHOSPHATE
2.5GM/PACKET
POWDER; ORAL
Discontinued
No
None
CALCIBIND
CELLULOSE SODIUM PHOSPHATE
300GM/BOT
POWDER; ORAL
Discontinued
No
None
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