DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CEFDINIR
FDA Application No:
(ANDA) 065259
Active Ingredient(s):
CEFDINIR
Company:
LUPIN
Original Approval or Tentative Approval Date:
May 31, 2006
Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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
CEFDINIR
CEFDINIR
125MG/5ML
FOR SUSPENSION; ORAL
Prescription
No
AB
CEFDINIR
CEFDINIR
250MG/5ML
FOR SUSPENSION; ORAL
Prescription
No
AB
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