bupropion hydrochloride

Generic: bupropion hydrochloride

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

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bupropion hydrochloride 100 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2577
Product ID 68071-2577_2c68b008-4863-51a9-e063-6294a90acc8b
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 680712577
Hyphenated Format 68071-2577

Supplemental Identifiers

RxCUI
993687
UPC
0368071257731
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
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (68071-2577-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68071-2577-9)
source: ndc

Packages (2)

68071-2577-3 30 TABLET, FILM COATED in 1 BOTTLE (68071-2577-3) 68071-2577-9 90 TABLET, FILM COATED in 1 BOTTLE (68071-2577-9)

Ingredients (1)

bupropion hydrochloride (100 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": "2c68b008-4863-51a9-e063-6294a90acc8b", "openfda": {"upc": ["0368071257731"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["d1043c87-0abe-ee8e-e053-2a95a90a419a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-2577-3)", "package_ndc": "68071-2577-3", "marketing_start_date": "20211117"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2577-9)", "package_ndc": "68071-2577-9", "marketing_start_date": "20250123"}], "brand_name": "Bupropion Hydrochloride", "product_id": "68071-2577_2c68b008-4863-51a9-e063-6294a90acc8b", "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": "68071-2577", "generic_name": "Bupropion Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}