Prescription Drug Information: Bupropion Hydrochloride (Page 7 of 7)

Package/Label Display Panel

Bupropion Hydrochloride Extended-Release Tablets, USP (SR)

150 mg

10 Tablets

bag label
(click image for full-size original)
BUPROPION HYDROCHLORIDE
bupropion hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:55154-7986(NDC:0904-6585)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BUPROPION HYDROCHLORIDE (BUPROPION) BUPROPION HYDROCHLORIDE 150 mg
Inactive Ingredients
Ingredient Name Strength
CARNAUBA WAX
FD&C BLUE NO. 2
FD&C RED NO. 40
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL, UNSPECIFIED
POLYSORBATE 80
TITANIUM DIOXIDE
HYPROMELLOSE, UNSPECIFIED
Product Characteristics
Color PURPLE Score no score
Shape ROUND Size 11mm
Flavor Imprint Code E;over;415
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:55154-7986-0 10 BLISTER PACK in 1 BAG contains a BLISTER PACK
1 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK This package is contained within the BAG (55154-7986-0)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075932 03/22/2004
Labeler — Cardinal Health (603638201)

Revised: 01/2021 Cardinal Health

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