Bupropion hydrochloride

Product NDC
71335-2649
11-digit product format
713352649
Labeler code
71335
Product ID
71335-2649_82d4ffc2-489f-4fee-acdf-ab5c72910464
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bupropion hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA216800
Marketing category
ANDA
Marketing start
2023-05-31
Substance
BUPROPION HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
ZG7E5POY8OBUPROPION HYDROCHLORIDE31677-93-7BUPROPION HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2649-17133526490160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-1) 2025-06-03NoNoHistorical
71335-2649-27133526490230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-2) 2025-06-03NoNoHistorical
71335-2649-371335264903100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-3) 2025-06-03NoNoHistorical
71335-2649-47133526490490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-4) 2025-06-03NoNoHistorical
71335-2649-571335264905120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-5) 2025-06-03NoNoHistorical
71335-2649-67133526490615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-6) 2025-06-03NoNoHistorical
71335-2649-77133526490721 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-7) 2025-06-03NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Bupropion hydrochlorideBryant Ranch Prepack2025-06-03HUMAN PRESCRIPTION DRUG LABEL1