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WellbutrinDrug - Wellbutrin The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Bupropion Hydrochloride
Strength -
100MG
Applicant -
GLAXOSMITHKLINE
New Drug Application (NDA) Number -
018644
Product Number -
003
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Dec 30, 1985
Reference Listed Drug (RLD) -
Yes
Type -
RX
Applicant Full Name -
Glaxosmithkline
Wellbutrin
Bupropion Hcl 100mg Tablet; Oral
Bupropion Hcl 75mg Tablet; Oral Wellbutrin 100mg Tablet; Oral Zyban 150mg Tablet, Extended Release; Oral Bupropion Hcl 100mg Tablet; Oral Bupropion Hcl 75mg Tablet; Oral Bupropion Hcl 100mg Tablet; Oral Bupropion Hcl 100mg Tablet; Oral Bupropion Hcl 75mg Tablet; Oral Bupropion Hcl 75mg Tablet; Oral NewDrugInformation |