bupropion

Generic: bupropion hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion
Generic Name bupropion hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

bupropion hydrochloride 150 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-565
Product ID 71205-565_64c33202-1fb1-4e0a-ae72-146375fa81aa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202304
Listing Expiration 2026-12-31
Marketing Start 2014-11-01

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 71205565
Hyphenated Format 71205-565

Supplemental Identifiers

RxCUI
993518
UPC
0371205565602
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 (source: ndc)
Generic Name bupropion hydrochloride (source: ndc)
Application Number ANDA202304 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-90)
source: ndc

Packages (3)

71205-565-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-30) 71205-565-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-60) 71205-565-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-90)

Ingredients (1)

bupropion hydrochloride (150 mg/1)

Linked Drug Pages (1)

bupropion ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "64c33202-1fb1-4e0a-ae72-146375fa81aa", "openfda": {"upc": ["0371205565602"], "unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["909204fc-ff55-43d9-b9ee-e607ef60965e"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-30)", "package_ndc": "71205-565-30", "marketing_start_date": "20210511"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-60)", "package_ndc": "71205-565-60", "marketing_start_date": "20210511"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-90)", "package_ndc": "71205-565-90", "marketing_start_date": "20210511"}], "brand_name": "bupropion", "product_id": "71205-565_64c33202-1fb1-4e0a-ae72-146375fa81aa", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71205-565", "generic_name": "bupropion hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA202304", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}