DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NAPROXEN SODIUM
FDA Application No:
(ANDA) 075168
Active Ingredient(s):
NAPROXEN SODIUM
Company:
DR REDDYS LABS INC
Label History
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 075168
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/28/1998
000
Approval
Letter
Therapeutic Equivalents
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