bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: quality care products, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler quality care products, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

bupropion hydrochloride 300 mg/1

Manufacturer
Quality Care Products, LLC

Identifiers & Regulatory

Product NDC 55700-820
Product ID 55700-820_56942110-9635-4106-a616-e227284026ab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210497
Marketing Start 2019-11-22
Marketing End 2026-08-31

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 55700820
Hyphenated Format 55700-820

Supplemental Identifiers

RxCUI
993557
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 ANDA210497 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-30)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-90)
source: ndc

Packages (2)

55700-820-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-30) 55700-820-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-90)

Ingredients (1)

bupropion hydrochloride (300 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": "56942110-9635-4106-a616-e227284026ab", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["a225dbbb-86f0-4547-a1c8-68eb64cd6892"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-30)", "package_ndc": "55700-820-30", "marketing_end_date": "20260831", "marketing_start_date": "20191122"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-90)", "package_ndc": "55700-820-90", "marketing_end_date": "20260331", "marketing_start_date": "20201112"}], "brand_name": "BUPROPION HYDROCHLORIDE", "product_id": "55700-820_56942110-9635-4106-a616-e227284026ab", "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": "55700-820", "generic_name": "BUPROPION HYDROCHLORIDE", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPROPION HYDROCHLORIDE", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA210497", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20191122"}