FDA.reportPublic FDA data

Bupropion Hydrochloride

Product NDC
60429-747
11-digit product format
604290747
Labeler code
60429
Product ID
60429-747_43e78c36-28fa-06c3-e063-6394a90a221b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bupropion Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Golden State Medical Supply, Inc.
Application
ANDA076143
Marketing category
ANDA
Marketing start
2006-01-17
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

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BUPROPION HYDROCHLORIDE100 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
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
60429-747-01Bupropion Hydrochloride100 in 1 BOTTLETABLET, FILM COATED1009

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60429-747BUPROPION HYDROCHLORIDE TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]7Current NDC, Legacy NDC, 1 package rows20240703_9490d611-b679-45c7-e053-2a95a90afb87.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
993687buPROPion HCl 100 MG Oral TabletPSN9490d611-b679-45c7-e053-2a95a90afb879
993691buPROPion HCl 75 MG Oral TabletPSN9490d611-b679-45c7-e053-2a95a90afb879
993687bupropion hydrochloride 100 MG Oral TabletSCD9490d611-b679-45c7-e053-2a95a90afb879
993691bupropion hydrochloride 75 MG Oral TabletSCD9490d611-b679-45c7-e053-2a95a90afb879
993691bupropion HCl 75 MG Oral TabletSY9490d611-b679-45c7-e053-2a95a90afb879
993687buPROPion HCl 100 MG Oral TabletPSN82b6e823-6b5d-4477-87c2-741cf46110151
993687buPROPion HCl 100 MG Oral TabletPSNb0e10a21-0ae3-4a8b-bd3e-7a48b30f84181
993687bupropion hydrochloride 100 MG Oral TabletSCD82b6e823-6b5d-4477-87c2-741cf46110151
993687bupropion hydrochloride 100 MG Oral TabletSCDb0e10a21-0ae3-4a8b-bd3e-7a48b30f84181

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
60429-747-0160429074701100 TABLET, FILM COATED in 1 BOTTLE (60429-747-01) 2019-08-220000-00-00NoNoCurrent