DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ANSPOR
FDA Application No:
(ANDA) 061866
Active Ingredient(s):
CEPHRADINE
Company:
GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:
October 15, 1974
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
ANSPOR
CEPHRADINE
125MG/5ML
FOR SUSPENSION; ORAL
Discontinued
No
None
ANSPOR
CEPHRADINE
250MG/5ML
FOR SUSPENSION; ORAL
Discontinued
No
None
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