bupropion hydrochloride xl (50090-7112)

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 50090-7112

Product ID 50090-7112_732484bd-0f31-4406-8429-dc70c3a570d0

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA210015

Listing Expiration 2026-12-31

Marketing Start 2023-04-30

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 500907112

Hyphenated Format 50090-7112

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 ANDA210015 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

150 mg/1

source: ndc

Packaging

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7112-0)

source: ndc

Packages (1)

50090-7112-0 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7112-0)

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": "732484bd-0f31-4406-8429-dc70c3a570d0", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["67590438-1f66-40ce-b595-8df760663671"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7112-0)", "package_ndc": "50090-7112-0", "marketing_start_date": "20240311"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "50090-7112_732484bd-0f31-4406-8429-dc70c3a570d0", "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": "50090-7112", "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": "ANDA210015", "marketing_category": "ANDA", "marketing_start_date": "20230430", "listing_expiration_date": "20261231"}