bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

bupropion hydrochloride 150 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8769
Product ID 68788-8769_17da2d67-85ad-4170-bd4e-1b9ca4565950
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216800
Listing Expiration 2027-12-31
Marketing Start 2024-11-19

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 687888769
Hyphenated Format 68788-8769

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 (source: ndc)
Generic Name bupropion hydrochloride (source: ndc)
Application Number ANDA216800 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-1)
  • 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-2)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-3)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-6)
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-8)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-9)
source: ndc

Packages (6)

68788-8769-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-1) 68788-8769-2 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-2) 68788-8769-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-3) 68788-8769-6 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-6) 68788-8769-8 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-8) 68788-8769-9 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-9)

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": "17da2d67-85ad-4170-bd4e-1b9ca4565950", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["093c4a61-02d9-4b55-b612-569aa25d3f2a"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-1)", "package_ndc": "68788-8769-1", "marketing_start_date": "20241119"}, {"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-2)", "package_ndc": "68788-8769-2", "marketing_start_date": "20241119"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-3)", "package_ndc": "68788-8769-3", "marketing_start_date": "20241119"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-6)", "package_ndc": "68788-8769-6", "marketing_start_date": "20241119"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-8)", "package_ndc": "68788-8769-8", "marketing_start_date": "20241119"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-9)", "package_ndc": "68788-8769-9", "marketing_start_date": "20241119"}], "brand_name": "Bupropion hydrochloride", "product_id": "68788-8769_17da2d67-85ad-4170-bd4e-1b9ca4565950", "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": "68788-8769", "generic_name": "Bupropion hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA216800", "marketing_category": "ANDA", "marketing_start_date": "20241119", "listing_expiration_date": "20271231"}