bupropion hydrochloride (xl) (50090-7110)

Drug Facts

Product Profile

Brand Name bupropion hydrochloride (xl)

Generic Name bupropion hydrochloride

Labeler a-s medication solutions

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

bupropion hydrochloride 150 mg/1

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7110

Product ID 50090-7110_4ecbc3fb-72e9-430a-9903-1da1e65ed1c7

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA210081

Listing Expiration 2026-12-31

Marketing Start 2018-08-30

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 500907110

Hyphenated Format 50090-7110

Supplemental Identifiers

RxCUI

993541

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 (xl) (source: ndc)

Generic Name bupropion hydrochloride (source: ndc)

Application Number ANDA210081 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

150 mg/1

source: ndc

Packaging

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-0)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-1)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-2)

source: ndc

Packages (3)

50090-7110-0 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-0) 50090-7110-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-1) 50090-7110-2 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-2)

Ingredients (1)

bupropion hydrochloride (150 mg/1)

Linked Drug Pages (1)

Bupropion Hydrochloride (XL) ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "4ecbc3fb-72e9-430a-9903-1da1e65ed1c7", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["8ae81b03-b447-4a3f-8ed9-ebf75ee52b49"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-0)", "package_ndc": "50090-7110-0", "marketing_start_date": "20240311"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-1)", "package_ndc": "50090-7110-1", "marketing_start_date": "20240311"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-2)", "package_ndc": "50090-7110-2", "marketing_start_date": "20240311"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "50090-7110_4ecbc3fb-72e9-430a-9903-1da1e65ed1c7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-7110", "generic_name": "bupropion hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "(XL)", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA210081", "marketing_category": "ANDA", "marketing_start_date": "20180830", "listing_expiration_date": "20261231"}