Bupropion Hydrochloride

Product NDC
72241-020
11-digit product format
722410020
Labeler code
72241
Product ID
72241-020_fe5a706a-47cf-47d4-a6ed-db4e7f08a169
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bupropion Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Modavar Pharmaceuticals LLC
Application
ANDA208606
Marketing category
ANDA
Marketing start
2020-01-16
Substance
BUPROPION HYDROCHLORIDE
Active strength
75 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

Additional Listing Data#

Finished product
Yes
Brand name base
Bupropion Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BUPROPION HYDROCHLORIDE75 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZG7E5POY8O
Rxcui993687, 993691

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4eceb285-f3c7-4092-a21a-4c9f3169f20cProduct name520260220
548ba7fd-fd0c-4a21-b2b0-d01bf93143b8Product name320240209
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
b8ee525f-67fb-39fb-91da-7e47ac54581dProduct name520200611
98e65af1-f5d0-75d5-c930-f8a4ce4c3284Product name920190211
e4d463bc-c674-43cb-be06-82786f310d01Product name120150326
0916dcfb-331f-89b1-8eac-6f7dc76d82daProduct name120140508
d7fc3d53-5a6c-de82-2808-1780f175f17eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72241-020-05Bupropion Hydrochloride100 in 1 BOTTLETABLET, FILM COATED1003
72241-020-11Bupropion Hydrochloride1000 in 1 BOTTLETABLET, FILM COATED10003
72241-020-17Bupropion Hydrochloride10 in 1 CARTONTABLET, FILM COATED103
72241-020-17Bupropion Hydrochloride10 in 1 BLISTER PACKTABLET, FILM COATED103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72241-020BUPROPION HYDROCHLORIDE TABLET, FILM COATED [MODAVAR PHARMACEUTICALS LLC]2Current NDC, Legacy NDC, 4 package rows20230215_0961f83e-25e9-4ffc-8669-44e4e9169978.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
993687buPROPion HCl 100 MG Oral TabletPSN0961f83e-25e9-4ffc-8669-44e4e91699783
993691buPROPion HCl 75 MG Oral TabletPSN0961f83e-25e9-4ffc-8669-44e4e91699783
993687bupropion hydrochloride 100 MG Oral TabletSCD0961f83e-25e9-4ffc-8669-44e4e91699783
993691bupropion hydrochloride 75 MG Oral TabletSCD0961f83e-25e9-4ffc-8669-44e4e91699783
993691bupropion HCl 75 MG Oral TabletSY0961f83e-25e9-4ffc-8669-44e4e91699783

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72241-020-0572241002005100 TABLET, FILM COATED in 1 BOTTLE (72241-020-05) 2023-01-120000-00-00NoNoCurrent
72241-020-11722410020111000 TABLET, FILM COATED in 1 BOTTLE (72241-020-11) 2023-01-120000-00-00NoNoCurrent
72241-020-177224100201710 BLISTER PACK in 1 CARTON (72241-020-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK10 blister pack2023-01-120000-00-00NoNoCurrent