DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GABAPENTIN
FDA Application No:
(ANDA) 077661
Active Ingredient(s):
GABAPENTIN
Company:
APOTEX INC
Original Approval or Tentative Approval Date:
September 13, 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
GABAPENTIN
GABAPENTIN
600MG
TABLET; ORAL
Prescription
No
AB
GABAPENTIN
GABAPENTIN
800MG
TABLET; ORAL
Prescription
No
AB
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