bupropion hydrochloride sr (50090-6871)

Drug Facts

Product Profile

Brand Name bupropion hydrochloride sr

Generic Name bupropion hydrochloride

Labeler a-s medication solutions

Dosage Form TABLET, FILM COATED, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

bupropion hydrochloride 150 mg/1

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6871

Product ID 50090-6871_65638420-ecfb-4cf3-af2a-59decc0fb8eb

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA205794

Listing Expiration 2026-12-31

Marketing Start 2018-04-20

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 500906871

Hyphenated Format 50090-6871

Supplemental Identifiers

RxCUI

993518

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 sr (source: ndc)

Generic Name bupropion hydrochloride (source: ndc)

Application Number ANDA205794 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

150 mg/1

source: ndc

Packaging

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-0)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-1)
180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-3)

source: ndc

Packages (4)

50090-6871-0 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-0) 50090-6871-1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-1) 50090-6871-2 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2) 50090-6871-3 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-3)

Ingredients (1)

bupropion hydrochloride (150 mg/1)

Linked Drug Pages (1)

Bupropion Hydrochloride SR ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "65638420-ecfb-4cf3-af2a-59decc0fb8eb", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["73167de9-948d-465c-88c0-c7743a79e7f5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-0)", "package_ndc": "50090-6871-0", "marketing_start_date": "20231204"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-1)", "package_ndc": "50090-6871-1", "marketing_start_date": "20231204"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2)", "package_ndc": "50090-6871-2", "marketing_start_date": "20231204"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-3)", "package_ndc": "50090-6871-3", "marketing_start_date": "20231204"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "50090-6871_65638420-ecfb-4cf3-af2a-59decc0fb8eb", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-6871", "generic_name": "bupropion hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205794", "marketing_category": "ANDA", "marketing_start_date": "20180420", "listing_expiration_date": "20261231"}