bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler bluepoint laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bupropion hydrochloride 300 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-614
Product ID 68001-614_48e4e5a0-3a1f-3aa1-e063-6394a90ad05f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215568
Listing Expiration 2027-12-31
Marketing Start 2024-04-09

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 68001614
Hyphenated Format 68001-614

Supplemental Identifiers

RxCUI
993541 993557
UNII
ZG7E5POY8O

Packaging Origin

Original Packager
true

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 ANDA215568 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (68001-614-03)
  • 30 TABLET in 1 BOTTLE (68001-614-04)
  • 90 TABLET in 1 BOTTLE (68001-614-05)
source: ndc

Packages (3)

68001-614-03 500 TABLET in 1 BOTTLE (68001-614-03) 68001-614-04 30 TABLET in 1 BOTTLE (68001-614-04) 68001-614-05 90 TABLET in 1 BOTTLE (68001-614-05)

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": "48e4e5a0-3a1f-3aa1-e063-6394a90ad05f", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541", "993557"], "spl_set_id": ["4956af38-182a-4015-a945-67e40bd38772"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (68001-614-03)", "package_ndc": "68001-614-03", "marketing_start_date": "20240409"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68001-614-04)", "package_ndc": "68001-614-04", "marketing_start_date": "20240620"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68001-614-05)", "package_ndc": "68001-614-05", "marketing_start_date": "20240620"}], "brand_name": "Bupropion hydrochloride", "product_id": "68001-614_48e4e5a0-3a1f-3aa1-e063-6394a90ad05f", "dosage_form": "TABLET", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "68001-614", "generic_name": "Bupropion hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA215568", "marketing_category": "ANDA", "marketing_start_date": "20240409", "listing_expiration_date": "20271231"}