bupropion hydrochloride

Generic: bupropion hydrochloride

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

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

bupropion hydrochloride 100 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-066
Product ID 31722-066_2d0de4b4-d4ee-3593-e063-6294a90ab0cc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216800
Listing Expiration 2026-12-31
Marketing Start 2023-05-31

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 31722066
Hyphenated Format 31722-066

Supplemental Identifiers

RxCUI
993503 993518 993536
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 ANDA216800 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-05)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-60)
source: ndc

Packages (3)

31722-066-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-01) 31722-066-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-05) 31722-066-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-60)

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": "2d0de4b4-d4ee-3593-e063-6294a90ab0cc", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993503", "993518", "993536"], "spl_set_id": ["f69b322b-93ab-407a-bf25-fe13c6896ca6"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-01)", "package_ndc": "31722-066-01", "marketing_start_date": "20230531"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-05)", "package_ndc": "31722-066-05", "marketing_start_date": "20230531"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-60)", "package_ndc": "31722-066-60", "marketing_start_date": "20230531"}], "brand_name": "Bupropion hydrochloride", "product_id": "31722-066_2d0de4b4-d4ee-3593-e063-6294a90ab0cc", "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": "31722-066", "generic_name": "Bupropion hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA216800", "marketing_category": "ANDA", "marketing_start_date": "20230531", "listing_expiration_date": "20261231"}