bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler micro labs limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bupropion hydrochloride 75 mg/1

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-241
Product ID 42571-241_42fa8097-2060-e261-e063-6294a90a6c29
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207403
Listing Expiration 2026-12-31
Marketing Start 2020-07-01

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 42571241
Hyphenated Format 42571-241

Supplemental Identifiers

RxCUI
993687 993691
UPC
0342571241018 0342571242015
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 ANDA207403 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (42571-241-01)
source: ndc

Packages (1)

42571-241-01 100 TABLET, FILM COATED in 1 BOTTLE (42571-241-01)

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": "42fa8097-2060-e261-e063-6294a90a6c29", "openfda": {"upc": ["0342571241018", "0342571242015"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["03450d2d-97ce-4518-af15-ab85b0d65d76"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42571-241-01)", "package_ndc": "42571-241-01", "marketing_start_date": "20200701"}], "brand_name": "BUPROPION HYDROCHLORIDE", "product_id": "42571-241_42fa8097-2060-e261-e063-6294a90a6c29", "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": "42571-241", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPROPION HYDROCHLORIDE", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA207403", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}