DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NAPROXEN SODIUM
FDA Application No:
(ANDA) 074789
Active Ingredient(s):
NAPROXEN SODIUM
Company:
LEINER
Original Approval or Tentative Approval Date:
February 27, 1997
Therapeutic Equivalents
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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
NAPROXEN SODIUM
NAPROXEN SODIUM
EQ 200MG BASE
TABLET; ORAL
OTC
No
None
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