DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
WELLBUTRIN SR
FDA Application No:
(NDA) 020358
Active Ingredient(s):
BUPROPION HYDROCHLORIDE
Company:
GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:
October 4, 1996
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Label Information
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
WELLBUTRIN SR
BUPROPION HYDROCHLORIDE
50MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
None
WELLBUTRIN SR
BUPROPION HYDROCHLORIDE
100MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB1
WELLBUTRIN SR
BUPROPION HYDROCHLORIDE
150MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
Yes
AB1
WELLBUTRIN SR
BUPROPION HYDROCHLORIDE
200MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB1
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