DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MANNITOL 25%
FDA Application No:
(ANDA) 087409
Active Ingredient(s):
MANNITOL
Company:
LUITPOLD
Original Approval or Tentative Approval Date:
January 21, 1982
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MANNITOL 25%
MANNITOL
12.5GM/50ML
INJECTABLE; INJECTION
Prescription
No
AP
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