Bupropion Hydrochloride SR (Page 10 of 10)

bupropion hydrochloride

Label ImageLabel Image
BUPROPION HYDROCHLORIDE SR bupropion hydrochloride tablet, film coated, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-1150(NDC:0591-3543)
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
HYDROXYPROPYL CELLULOSE (160000 WAMW)
MICROCRYSTALLINE CELLULOSE 101
SILICON DIOXIDE
STEARIC ACID
MAGNESIUM STEARATE
HYDROCHLORIC ACID
LACTOSE MONOHYDRATE
HYDROXYPROPYL CELLULOSE, UNSPECIFIED
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL 400
Product Characteristics
Color white (white to off-white) Score no score
Shape ROUND Size 11mm
Flavor Imprint Code WPI;867
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-1150-0 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC None
2 NDC:50090-1150-1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA079094 06/11/2009
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-1150), REPACK (50090-1150)

Revised: 07/2022 A-S Medication Solutions

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