DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
KEFTAB
FDA Application No:
(NDA) 050614
Active Ingredient(s):
CEPHALEXIN HYDROCHLORIDE
Company:
LILLY
Original Approval or Tentative Approval Date:
October 29, 1987
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no 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
KEFTAB
CEPHALEXIN HYDROCHLORIDE
EQ 250MG BASE
TABLET; ORAL
Discontinued
No
None
KEFTAB
CEPHALEXIN HYDROCHLORIDE
EQ 500MG BASE
TABLET; ORAL
Discontinued
No
None
KEFTAB
CEPHALEXIN HYDROCHLORIDE
EQ 333MG BASE
TABLET; ORAL
Discontinued
No
None
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