FDA.reportPublic FDA data

Bupropion Hydrochloride

Product NDC
72162-1527
11-digit product format
721621527
Labeler code
72162
Product ID
72162-1527_50e8778b-87dc-49dc-985b-b2b9f05d5b1a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
bupropion hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA207479
Marketing category
ANDA
Marketing start
2017-04-12
Substance
BUPROPION HYDROCHLORIDE
Active strength
300 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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Bupropion Hydrochloride
Brand name suffix
(XL)
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BUPROPION HYDROCHLORIDE300 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZG7E5POY8O
Rxcui993557

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
72162-1527-3Bupropion Hydrochloride(XL)30 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE30101
72162-1527-5Bupropion Hydrochloride(XL)500 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE500101

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1527-3EA - Each72162-15278bbd4445-4407-439c-a5d1-fe1f782d399c12024-03-12
72162-1527-5EA - Each72162-1527e248f0cc-7a19-49bb-837e-0e47b58c45ff12024-03-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1527BUPROPION HYDROCHLORIDE (XL) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]100Current NDC, 2 package rows20240124_a7553281-be90-47e3-8d2b-b027f6d18d3a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
993557buPROPion HCl 300 MG 24HR Extended Release Oral TabletPSNa7553281-be90-47e3-8d2b-b027f6d18d3a101
99355724 HR bupropion hydrochloride 300 MG Extended Release Oral TabletSCDa7553281-be90-47e3-8d2b-b027f6d18d3a101
993557bupropion HCl XL 300 MG 24 HR Extended Release Oral TabletSYa7553281-be90-47e3-8d2b-b027f6d18d3a101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
72162-1527-37216215270330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1527-3) 2017-04-12NoNoHistorical
72162-1527-572162152705500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1527-5) 2017-04-12NoNoHistorical