DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FERRLECIT
FDA Application No:
(NDA) 020955
Active Ingredient(s):
SODIUM FERRIC GLUCONATE COMPLEX
Company:
WATSON PHARMS
Original Approval or Tentative Approval Date:
February 18, 1999
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
Label Information
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
FERRLECIT
SODIUM FERRIC GLUCONATE COMPLEX
62.5MG/5ML
INJECTABLE; INJECTION
Prescription
Yes
None
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