NDC 55648-105

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 Wockhardt Limited. The primary component is Bupropion Hydrochloride.

Product ID55648-105_572fcaa4-314e-42b2-aa6b-f5ec54da6199
NDC55648-105
Product TypeHuman Prescription Drug
Proprietary NameBupropion Hydrochloride (SR)
Generic NameBupropion Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2012-08-30
Marketing CategoryANDA / ANDA
Application NumberANDA201331
Labeler NameWockhardt Limited
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 55648-105-03

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-105-03)
Marketing Start Date2012-08-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55648-105-01 [55648010501]

Bupropion Hydrochloride (SR) TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA201331
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-08-30
Inactivation Date2020-01-31

NDC 55648-105-03 [55648010503]

Bupropion Hydrochloride (SR) TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA201331
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-08-30
Inactivation Date2020-01-31

NDC 55648-105-02 [55648010502]

Bupropion Hydrochloride (SR) TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA201331
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-08-30
Inactivation Date2020-01-31

NDC 55648-105-07 [55648010507]

Bupropion Hydrochloride (SR) TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA201331
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-11-07

NDC 55648-105-05 [55648010505]

Bupropion Hydrochloride (SR) TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA201331
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-11-07
Inactivation Date2020-01-31

NDC 55648-105-04 [55648010504]

Bupropion Hydrochloride (SR) TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA201331
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-11-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BUPROPION HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:1a2a5385-ec04-448f-8bdb-d1cc3eb5f1c0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 993518
  • 993536
  • 993503
    • UPC Code
  • 0364679105023
  • 0364679101018
  • 0364679107034

    • 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
    69097-879BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    69097-878BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    69097-877BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    70518-1033BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    70934-156BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    71335-0006BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    71335-0025BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    45865-633BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    50090-3453BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    50090-3249BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    53002-1509BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    55648-107Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    55648-105Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    55648-101Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    58118-0878BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    64679-105Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    64679-101Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    64679-107Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    43598-863BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    50228-338Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    70518-2648BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    50090-5101BUPROPION HYDROCHLORIDE (SR)BUPROPION 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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