bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bupropion hydrochloride 75 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-774
Product ID 71610-774_edf166e7-bcf0-4bda-97ea-d9b82140aab3
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 71610774
Hyphenated Format 71610-774

Supplemental Identifiers

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

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71610-774-70)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80)
  • 360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94)
source: ndc

Packages (4)

71610-774-53 60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53) 71610-774-70 120 TABLET, FILM COATED in 1 BOTTLE (71610-774-70) 71610-774-80 180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80) 71610-774-94 360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94)

Ingredients (1)

bupropion hydrochloride (75 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": "edf166e7-bcf0-4bda-97ea-d9b82140aab3", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["8d80f882-1887-4d73-b09f-e98fd7ef2acb"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53)", "package_ndc": "71610-774-53", "marketing_start_date": "20240122"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71610-774-70)", "package_ndc": "71610-774-70", "marketing_start_date": "20240125"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80)", "package_ndc": "71610-774-80", "marketing_start_date": "20240125"}, {"sample": false, "description": "360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94)", "package_ndc": "71610-774-94", "marketing_start_date": "20240125"}], "brand_name": "Bupropion Hydrochloride", "product_id": "71610-774_edf166e7-bcf0-4bda-97ea-d9b82140aab3", "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": "71610-774", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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"}