bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bupropion hydrochloride 100 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-390
Product ID 51655-390_49dba4c8-2aab-fab0-e063-6294a90aca6d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206975
Listing Expiration 2027-12-31
Marketing Start 2022-01-28

Pharmacologic Class

Classes
aminoketone [epc] dopamine uptake inhibitors [moa] increased dopamine activity [pe] increased norepinephrine activity [pe] norepinephrine uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655390
Hyphenated Format 51655-390

Supplemental Identifiers

RxCUI
993687
UNII
ZG7E5POY8O

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name bupropion hydrochloride (source: ndc)
Generic Name bupropion hydrochloride (source: ndc)
Application Number ANDA206975 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE, PLASTIC (51655-390-25)
  • 90 TABLET in 1 BOTTLE, PLASTIC (51655-390-26)
source: ndc

Packages (2)

51655-390-25 60 TABLET in 1 BOTTLE, PLASTIC (51655-390-25) 51655-390-26 90 TABLET in 1 BOTTLE, PLASTIC (51655-390-26)

Ingredients (1)

bupropion hydrochloride (100 mg/1)

Linked Drug Pages (1)

bupropion Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49dba4c8-2aab-fab0-e063-6294a90aca6d", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["d9bbacb3-63b4-2922-e053-2a95a90a6085"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-390-25)", "package_ndc": "51655-390-25", "marketing_start_date": "20220128"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-390-26)", "package_ndc": "51655-390-26", "marketing_start_date": "20220128"}], "brand_name": "bupropion Hydrochloride", "product_id": "51655-390_49dba4c8-2aab-fab0-e063-6294a90aca6d", "dosage_form": "TABLET", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "51655-390", "generic_name": "bupropion Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20220128", "listing_expiration_date": "20271231"}