DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NALFON
FDA Application No:
(NDA) 017604
Active Ingredient(s):
FENOPROFEN CALCIUM
Company:
PEDINOL
Original Approval or Tentative Approval Date:
March 16, 1976
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
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
NALFON
FENOPROFEN CALCIUM
EQ 300MG BASE
CAPSULE; ORAL
Prescription
Yes
AB
NALFON 200
FENOPROFEN CALCIUM
EQ 200MG BASE
CAPSULE; ORAL
Prescription
No
AB
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