NDC 68071-2192

Bupropion Hydrochloride SR

Bupropion Hydrochloride

Bupropion Hydrochloride SR is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals, Inc.. The primary component is Bupropion Hydrochloride.

Product ID68071-2192_4bcdf2c6-dc1e-558f-e054-00144ff8d46c
NDC68071-2192
Product TypeHuman Prescription Drug
Proprietary NameBupropion Hydrochloride SR
Generic NameBupropion Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2009-07-02
Marketing CategoryANDA / ANDA
Application NumberANDA079095
Labeler NameNuCare Pharmaceuticals, Inc.
Substance NameBUPROPION HYDROCHLORIDE
Active Ingredient Strength150 mg/1
Pharm ClassesAminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68071-2192-9

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-2192-9)
Marketing Start Date2017-03-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68071-2192-6 [68071219206]

Bupropion Hydrochloride SR TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA079095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-28
Marketing End Date2019-12-31
Inactivation Date2020-01-31
Reactivation Date2020-05-05

NDC 68071-2192-3 [68071219203]

Bupropion Hydrochloride SR TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA079095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-28
Marketing End Date2019-12-31
Inactivation Date2020-01-31
Reactivation Date2020-05-05

NDC 68071-2192-9 [68071219209]

Bupropion Hydrochloride SR TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA079095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-28
Marketing End Date2019-12-31
Inactivation Date2020-01-31
Reactivation Date2020-05-05

Drug Details

Active Ingredients

IngredientStrength
BUPROPION HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:4bcdf2c6-dc1d-558f-e054-00144ff8d46c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 993518

    • Pharmacological Class

    • Aminoketone [EPC]
    • Dopamine Uptake Inhibitors [MoA]
    • Increased Dopamine Activity [PE]
    • Increased Norepinephrine Activity [PE]
    • Norepinephrine Uptake Inhibitors [MoA]

    NDC Crossover Matching brand name "Bupropion Hydrochloride SR" or generic name "Bupropion Hydrochloride"

    NDCBrand NameGeneric Name
    68071-2192Bupropion Hydrochloride SRBupropion Hydrochloride SR
    68788-7174Bupropion Hydrochloride SRBupropion Hydrochloride SR
    0591-3540Bupropion Hydrochloride SRBupropion Hydrochloride SR
    0591-3543Bupropion Hydrochloride SRBupropion Hydrochloride SR
    0591-3541Bupropion Hydrochloride SRBupropion Hydrochloride SR
    0591-3542Bupropion Hydrochloride SRBupropion Hydrochloride SR
    71335-0135Bupropion Hydrochloride SRBupropion Hydrochloride SR
    71335-0314Bupropion Hydrochloride SRBupropion Hydrochloride SR
    0615-7904Bupropion Hydrochloride SRBupropion Hydrochloride SR
    43063-744BUPROPION HYDROCHLORIDE SRBUPROPION HYDROCHLORIDE SR
    43063-913Bupropion Hydrochloride SRBupropion Hydrochloride SR
    43598-536Bupropion Hydrochloride SRBupropion Hydrochloride SR
    43598-538Bupropion Hydrochloride SRBupropion Hydrochloride SR
    43598-537Bupropion Hydrochloride SRBupropion Hydrochloride SR
    43598-753Bupropion Hydrochloride SRBupropion Hydrochloride SR
    43598-752Bupropion Hydrochloride SRBupropion Hydrochloride SR
    43598-751Bupropion Hydrochloride SRBupropion Hydrochloride SR
    45865-885Bupropion Hydrochloride SRBupropion Hydrochloride SR
    50090-1150Bupropion Hydrochloride SRBupropion Hydrochloride SR
    50090-0861Bupropion Hydrochloride SRBupropion Hydrochloride SR
    50090-2584Bupropion Hydrochloride SRBupropion Hydrochloride SR
    50228-174Bupropion Hydrochloride SRBupropion Hydrochloride SR
    50228-176Bupropion Hydrochloride SRBupropion Hydrochloride SR
    50228-175Bupropion Hydrochloride SRBupropion Hydrochloride SR
    50436-3541Bupropion Hydrochloride SRBupropion Hydrochloride SR
    53002-1345Bupropion Hydrochloride SRBupropion Hydrochloride SR
    55700-028Bupropion Hydrochloride SRBupropion Hydrochloride SR
    60429-217Bupropion Hydrochloride SRBupropion Hydrochloride SR
    60429-218Bupropion Hydrochloride SRBupropion Hydrochloride SR
    60429-216Bupropion Hydrochloride SRBupropion Hydrochloride SR
    63187-566Bupropion Hydrochloride SRBupropion Hydrochloride SR
    63187-726Bupropion Hydrochloride SRBupropion Hydrochloride SR
    63187-952Bupropion Hydrochloride SRBupropion Hydrochloride SR
    63629-6438Bupropion Hydrochloride SRBupropion Hydrochloride SR
    70518-2029Bupropion Hydrochloride SRBupropion Hydrochloride SR
    70934-225Bupropion Hydrochloride SRBupropion Hydrochloride SR
    70934-277Bupropion Hydrochloride SRBupropion Hydrochloride SR
    70518-2297Bupropion Hydrochloride SRBupropion Hydrochloride SR
    0115-5445Bupropion HydrochlorideBUPROPION HYDROCHLORIDE
    0115-6811Bupropion HydrochlorideBUPROPION HYDROCHLORIDE
    0185-0410Bupropion HydrochlorideBupropion Hydrochloride
    0185-0415Bupropion HydrochlorideBupropion Hydrochloride
    0185-1111Bupropion HydrochlorideBupropion Hydrochloride
    0173-0135WELLBUTRINbupropion hydrochloride
    0173-0722WELLBUTRINbupropion hydrochloride
    0173-0947WELLBUTRINbupropion hydrochloride
    0173-0556ZYBANbupropion hydrochloride
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