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Bupropion - Medication Information

Product NDC Code 65841-780
Drug Name

Bupropion

Type Generic
Pharm Class Aminoketone [EPC],
Dopamine Uptake Inhibitors [MoA],
Increased Dopamine Activity [PE],
Increased Norepinephrine Activity [PE],
Norepinephrine Uptake Inhibitors [MoA]
Active Ingredients
Bupropion hydrochloride 300 mg/1
Route ORAL
Dosage Form TABLET, EXTENDED RELEASE
RxCUI drug identifier 993541,
993557
Application Number ANDA201567
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
65841-780-05 500 tablet, extended release in 1 bottle (65841-780-05)
65841-780-06 30 tablet, extended release in 1 bottle (65841-780-06)
65841-780-10 1000 tablet, extended release in 1 bottle (65841-780-10)
65841-780-16 90 tablet, extended release in 1 bottle (65841-780-16)
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Spl product data elements

Usually a list of ingredients in a drug product.
bupropion bupropion BUPROPION HYDROCHLORIDE BUPROPION HYPROMELLOSES MAGNESIUM STEARATE METHACRYLIC ACID POLYETHYLENE GLYCOL, UNSPECIFIED TRIETHYL CITRATE POVIDONE ETHYLCELLULOSES SILICON DIOXIDE BUTYL ALCOHOL FERROSOFERRIC OXIDE ISOPROPYL ALCOHOL PROPYLENE GLYCOL SHELLAC AMMONIA CREAMY WHITE TO PALE YELLOW ROUND 354 bupropion bupropion BUPROPION HYDROCHLORIDE BUPROPION HYPROMELLOSES MAGNESIUM STEARATE POLYETHYLENE GLYCOL, UNSPECIFIED METHACRYLIC ACID TRIETHYL CITRATE POVIDONE ETHYLCELLULOSES SILICON DIOXIDE BUTYL ALCOHOL FERROSOFERRIC OXIDE ISOPROPYL ALCOHOL PROPYLENE GLYCOL SHELLAC AMMONIA CREAMY WHITE TO PALE YELLOW ROUND 353

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 65841-780-05 Bupropion Hydrochloride Extended-release Tablets USP (XL), 300 mg 500 Tablets Rx only NDC 65841-836-05 Bupropion Hydrochloride Extended-release Tablets USP (XL), 150 mg 500 Tablets Rx only Bupropion hydrochloride extended-release tablets, USP (XL) label

Spl medguide

Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.
Manufactured by: Cadila Healthcare Ltd. India. SPL MEDGUIDE

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API