Bupropion Hydrochloride

Product NDC: 51407-206
11-digit product format: 514070206
Labeler code: 51407
Product ID: 51407-206_447188f5-1076-885a-e063-6294a90ae7c5
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: bupropion hydrochloride
Dosage form: TABLET, EXTENDED RELEASE
Route: ORAL
Labeler: Golden State Medical Supply, Inc.
Application: ANDA210081
Marketing category: ANDA
Marketing start: 2017-11-03
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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
4eceb285-f3c7-4092-a21a-4c9f3169f20c	Product name	5	20260220
548ba7fd-fd0c-4a21-b2b0-d01bf93143b8	Product name	3	20240209
43a1ed49-eae2-4840-8075-cb4b33478540	Product name	1	20230425
b8ee525f-67fb-39fb-91da-7e47ac54581d	Product name	5	20200611
98e65af1-f5d0-75d5-c930-f8a4ce4c3284	Product name	9	20190211
e4d463bc-c674-43cb-be06-82786f310d01	Product name	1	20150326
0916dcfb-331f-89b1-8eac-6f7dc76d82da	Product name	1	20140508
d7fc3d53-5a6c-de82-2808-1780f175f17e	Product name	1	20140508

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51407-206-05	Bupropion Hydrochloride(XL)	500 in 1 BOTTLE, PLASTIC	TABLET, EXTENDED RELEASE	500	8
51407-206-30	Bupropion Hydrochloride(XL)	30 in 1 BOTTLE, PLASTIC	TABLET, EXTENDED RELEASE	30	8
51407-206-90	Bupropion Hydrochloride(XL)	90 in 1 BOTTLE, PLASTIC	TABLET, EXTENDED RELEASE	90	8

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51407-206-05	EA - Each	51407-206	03876839-902a-4418-982f-d910f522dfb1	1	2019-05-02
51407-206-30	EA - Each	51407-206	9dd517e6-ec95-4f61-9af1-3d4c98d1a670	1	2019-05-02
51407-206-90	EA - Each	51407-206	66ad4278-3338-4f3c-9d5f-4f82d2c62a59	1	2019-05-02

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51407-206	BUPROPION HYDROCHLORIDE (XL) (BUPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [GOLDEN STATE MEDICAL SUPPLY, INC.]	7	Current NDC, Legacy NDC, 3 package rows	20241027_8722a60e-7635-7455-e053-2991aa0abaf7.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
ZG7E5POY8O	BUPROPION HYDROCHLORIDE	31677-93-7	BUPROPION HYDROCHLORIDE

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
993541	buPROPion HCl 150 MG 24HR Extended Release Oral Tablet	PSN	38aecc00-de96-4479-aa9b-5d09a1529642	1
993541	24 HR bupropion hydrochloride 150 MG Extended Release Oral Tablet	SCD	38aecc00-de96-4479-aa9b-5d09a1529642	1
993541	bupropion HCl XL 150 MG 24 HR Extended Release Oral Tablet	SY	38aecc00-de96-4479-aa9b-5d09a1529642	1

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
51407-206-05	51407020605	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-206-05)	2019-02-25	0000-00-00	No	No	Current
51407-206-30	51407020630	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-206-30)	2019-02-25	0000-00-00	No	No	Current
51407-206-90	51407020690	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-206-90)	2019-02-25	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Bupropion Hydrochloride (XL)	Golden State Medical Supply, Inc.	2025-11-25	HUMAN PRESCRIPTION DRUG LABEL	8
Bupropion Hydrochloride (XL)	Aphena Pharma Solutions - Tennessee, LLC	2019-10-09	HUMAN PRESCRIPTION DRUG LABEL	1