bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bupropion hydrochloride 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1869
Product ID 50090-1869_aa89dc60-57fd-465a-9c47-8aa53221bd91
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076143
Listing Expiration 2026-12-31
Marketing Start 2006-01-17

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 500901869
Hyphenated Format 50090-1869

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 ANDA076143 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-1869-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-1869-3)
source: ndc

Packages (2)

50090-1869-0 60 TABLET, FILM COATED in 1 BOTTLE (50090-1869-0) 50090-1869-3 90 TABLET, FILM COATED in 1 BOTTLE (50090-1869-3)

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": "aa89dc60-57fd-465a-9c47-8aa53221bd91", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["78ef709a-f835-4b03-92dd-16a4c82af0c1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-1869-0)", "package_ndc": "50090-1869-0", "marketing_start_date": "20150610"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-1869-3)", "package_ndc": "50090-1869-3", "marketing_start_date": "20150610"}], "brand_name": "Bupropion Hydrochloride", "product_id": "50090-1869_aa89dc60-57fd-465a-9c47-8aa53221bd91", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-1869", "generic_name": "Bupropion Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}