Bupropion Hydrochloride

Product NDC
63187-713
11-digit product format
631870713
Labeler code
63187
Product ID
63187-713_b5525d33-534c-440c-8a04-df329fc85056
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
BUPROPION HYDROCHLORIDE
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA077415
Marketing category
ANDA
Marketing start
2009-05-01
Substance
BUPROPION HYDROCHLORIDE
Active strength
150 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 HYDROCHLORIDE150 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZG7E5POY8O
Rxcui993541

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
63187-713-30Bupropion Hydrochloride30 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE303
63187-713-60Bupropion Hydrochloride60 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE603
63187-713-90Bupropion Hydrochloride90 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE903

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63187-713-30EA - Each63187-713e50d9aee-9411-4ec8-b918-e6b159eb450812023-08-08
63187-713-90EA - Each63187-713b43af4fd-be95-4f37-8908-543fc6b62f7a12018-06-11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63187-713BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [PROFICIENT RX LP]3Current NDC, Legacy NDC, 3 package rows20210112_e57451fd-aba5-47d6-9892-ffe2a6021b6f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
993541buPROPion HCl 150 MG 24HR Extended Release Oral TabletPSNe57451fd-aba5-47d6-9892-ffe2a6021b6f3
99354124 HR bupropion hydrochloride 150 MG Extended Release Oral TabletSCDe57451fd-aba5-47d6-9892-ffe2a6021b6f3
993541bupropion HCl XL 150 MG 24 HR Extended Release Oral TabletSYe57451fd-aba5-47d6-9892-ffe2a6021b6f3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63187-713-306318707133030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-30) 2016-06-010000-00-00NoNoCurrent
63187-713-606318707136060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-60) 2016-06-010000-00-00NoNoCurrent
63187-713-906318707139090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-90) 2016-06-010000-00-00NoNoCurrent