Home NDC 68084-252-11 NDC 68084-252-11 - Bupropion Hydrochloride This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 68084-252
Requested NDC 68084-252-11
Package NDCs from labels 68084-252-11, 68084-252-21
Manufacturer American Health Packaging
Effective date 2024-05-03
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BUPROPION HYDROCHLORIDE ACTIVE INGREDIENT ZG7E5POY8O BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 BUPROPION ACTIVE MOIETY 01ZG3TPX31 BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 ALCOHOL INACTIVE INGREDIENT 3K9958V90M BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 ETHYLCELLULOSES INACTIVE INGREDIENT 7Z8S9VYZ4B BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 HYDROGENATED COTTONSEED OIL INACTIVE INGREDIENT Z82Y2C65EA BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 HYDROXYPROPYL CELLULOSE (TYPE H) INACTIVE INGREDIENT RFW2ET671P BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 ISOPROPYL ALCOHOL INACTIVE INGREDIENT ND2M416302 BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A INACTIVE INGREDIENT NX76LV5T8J BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 POVIDONES INACTIVE INGREDIENT FZ989GH94E BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] 6
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 57 of 218 · 4,352 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti Bacterial Hand Gel Midnight Blue Citrus ALCOHOL Bath & Body Works, Inc. 2b116b79-fe71-325a-e063-6394a90a045b 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Warm Vanilla Sugar ALCOHOL Bath & Body Works, Inc. 38d6f6a0-52bf-df77-e063-6394a90a4464 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Crystal Blue Coast ALCOHOL Bath & Body Works, Inc. 38e1480e-d217-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Raspberry Tangerine ALCOHOL Bath & Body Works, Inc. 38e1cc04-7905-74e4-e063-6394a90a7b4c 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Backyard Honeysuckle ALCOHOL Bath & Body Works, Inc. 38e1480e-d21c-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 38e1480e-d21d-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Raspberries and Whipped Vanilla ALCOHOL Bath & Body Works, Inc. 38e1cef4-4814-745c-e063-6394a90aebf0 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fiji White Sands ALCOHOL Bath & Body Works, Inc. 38e1c1d6-6505-4066-e063-6294a90ad3f4 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweetest Song ALCOHOL Bath & Body Works, Inc. 38e1d907-75d7-3906-e063-6294a90a2ed7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Endless Weekend ALCOHOL Bath & Body Works, Inc. 38e15918-9ee2-4061-e063-6294a90a881c 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pina Colada Swirl ALCOHOL Bath & Body Works, Inc. 38e1e122-2087-90fa-e063-6394a90ab625 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Eucalyptus and Spearmint ALCOHOL Bath & Body Works, Inc. 38e1f8da-2003-80ba-e063-6394a90a2d1d 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweet Orange and Agave ALCOHOL Bath & Body Works, Inc. 38e1d8fc-6f10-49d6-e063-6294a90a25ab 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Book Loft ALCOHOL Bath & Body Works, Inc. 38e1d8fc-6f11-49d6-e063-6294a90a25ab 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Turquoise Waters ALCOHOL Bath & Body Works, Inc. 38e1d9e9-08e7-3908-e063-6294a90adf6b 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sunlit Palm Trees ALCOHOL Bath & Body Works, Inc. 38e1d907-75d0-3906-e063-6294a90a2ed7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Watermelon ALCOHOL Bath & Body Works, Inc. 38e1f4cd-7707-404a-e063-6294a90afc92 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Pineapple Sunrise ALCOHOL Bath & Body Works, Inc. 38e1d8fc-6f12-49d6-e063-6294a90a25ab 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Beach Weather ALCOHOL Bath & Body Works, Inc. 38e1dc79-bdc3-3b84-e063-6294a90a61d7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Amalfi Lemon ALCOHOL Bath & Body Works, Inc. 38e1f158-187c-3b86-e063-6294a90a396f 2026-03-09 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.