bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bupropion hydrochloride 75 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0791
Product ID 71335-0791_ad6eaa94-18cd-495a-9a26-53dbd20a5a74
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206975
Listing Expiration 2026-12-31
Marketing Start 2016-08-19

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 713350791
Hyphenated Format 71335-0791

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 ANDA206975 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0791-1)
  • 60 TABLET in 1 BOTTLE (71335-0791-2)
  • 90 TABLET in 1 BOTTLE (71335-0791-3)
  • 7 TABLET in 1 BOTTLE (71335-0791-4)
  • 14 TABLET in 1 BOTTLE (71335-0791-5)
  • 120 TABLET in 1 BOTTLE (71335-0791-6)
  • 100 TABLET in 1 BOTTLE (71335-0791-7)
source: ndc

Packages (7)

71335-0791-1 30 TABLET in 1 BOTTLE (71335-0791-1) 71335-0791-2 60 TABLET in 1 BOTTLE (71335-0791-2) 71335-0791-3 90 TABLET in 1 BOTTLE (71335-0791-3) 71335-0791-4 7 TABLET in 1 BOTTLE (71335-0791-4) 71335-0791-5 14 TABLET in 1 BOTTLE (71335-0791-5) 71335-0791-6 120 TABLET in 1 BOTTLE (71335-0791-6) 71335-0791-7 100 TABLET in 1 BOTTLE (71335-0791-7)

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": "ad6eaa94-18cd-495a-9a26-53dbd20a5a74", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["144379e1-93b7-41c1-bc3a-7bdec5afa309"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0791-1)", "package_ndc": "71335-0791-1", "marketing_start_date": "20180426"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0791-2)", "package_ndc": "71335-0791-2", "marketing_start_date": "20190619"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0791-3)", "package_ndc": "71335-0791-3", "marketing_start_date": "20190619"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (71335-0791-4)", "package_ndc": "71335-0791-4", "marketing_start_date": "20190619"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-0791-5)", "package_ndc": "71335-0791-5", "marketing_start_date": "20190619"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0791-6)", "package_ndc": "71335-0791-6", "marketing_start_date": "20190619"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0791-7)", "package_ndc": "71335-0791-7", "marketing_start_date": "20190619"}], "brand_name": "bupropion Hydrochloride", "product_id": "71335-0791_ad6eaa94-18cd-495a-9a26-53dbd20a5a74", "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": "71335-0791", "generic_name": "bupropion Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20160819", "listing_expiration_date": "20261231"}