BUPROPION HYDROCHLORIDE

Generic: BUPROPION HYDROCHLORIDE

Labeler: Quality Care Products, LLC
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

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 150 mg/1

Identifiers & Regulatory

Product NDC 55700-849
Product ID 55700-849_bbb443b1-e9c5-4dd5-ade3-365f1faa2151
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210497
Marketing Start 2020-03-16
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55700849
Hyphenated Format 55700-849

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
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-849-30)
source: ndc

Packages (1)

55700-849-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-849-30)

Ingredients (1)

BUPROPION HYDROCHLORIDE (150 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": "bbb443b1-e9c5-4dd5-ade3-365f1faa2151", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["5301bc62-888a-4151-8938-d61f0e52bb45"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-849-30)", "package_ndc": "55700-849-30", "marketing_end_date": "20260228", "marketing_start_date": "20200316"}], "brand_name": "BUPROPION HYDROCHLORIDE", "product_id": "55700-849_bbb443b1-e9c5-4dd5-ade3-365f1faa2151", "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": "55700-849", "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": "150 mg/1"}], "application_number": "ANDA210497", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20200316"}