bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: apotex corp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler apotex corp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bupropion hydrochloride 75 mg/1

Manufacturer
Apotex Corp

Identifiers & Regulatory

Product NDC 60505-0158
Product ID 60505-0158_cf3f7cdc-3541-a71a-08c5-a74345180a3e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076143
Listing Expiration 2026-12-31
Marketing Start 2006-01-17

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 605050158
Hyphenated Format 60505-0158

Supplemental Identifiers

RxCUI
993687 993691
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 ANDA076143 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (60505-0158-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (60505-0158-3)
  • 500 TABLET, FILM COATED in 1 BOTTLE (60505-0158-5)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0158-7)
  • 90 TABLET, FILM COATED in 1 BOTTLE (60505-0158-9)
source: ndc

Packages (5)

Ingredients (1)

bupropion hydrochloride (75 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf3f7cdc-3541-a71a-08c5-a74345180a3e", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["86530199-999b-9f92-b1bc-b8515ec829f3"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60505-0158-1)", "package_ndc": "60505-0158-1", "marketing_start_date": "20060117"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-0158-3)", "package_ndc": "60505-0158-3", "marketing_start_date": "20060117"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (60505-0158-5)", "package_ndc": "60505-0158-5", "marketing_start_date": "20060117"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60505-0158-7)", "package_ndc": "60505-0158-7", "marketing_start_date": "20060117"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (60505-0158-9)", "package_ndc": "60505-0158-9", "marketing_start_date": "20060117"}], "brand_name": "Bupropion Hydrochloride", "product_id": "60505-0158_cf3f7cdc-3541-a71a-08c5-a74345180a3e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "60505-0158", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}