DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LIORESAL
FDA Application No:
(NDA) 017851
Active Ingredient(s):
BACLOFEN
Company:
NOVARTIS
Original Approval or Tentative Approval Date:
November 22, 1977
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
LIORESAL
BACLOFEN
10MG
TABLET; ORAL
Discontinued
No
None
LIORESAL
BACLOFEN
20MG
TABLET; ORAL
Discontinued
No
None
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