DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
BUTABARBITAL SODIUM
FDA Application No:
(ANDA) 085383
Active Ingredient(s):
BUTABARBITAL SODIUM
Company:
MORTON GROVE
Original Approval or Tentative Approval Date:
February 26, 1979
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
BUTABARBITAL SODIUM
BUTABARBITAL SODIUM
30MG/5ML
ELIXIR; ORAL
Discontinued
No
None
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