Bupropion Hydrochloride

Product NDC: 51655-003
11-digit product format: 516550003
Labeler code: 51655
Product ID: 51655-003_cdec0059-c52f-4f86-8935-ae5da1f1b8c6
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Bupropion Hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA078866
Marketing category: ANDA
Marketing start: 2014-06-01
Marketing end: 0000-00-00
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: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-003-26	2026-01-13	C162847	48780-1	9d75b9d1-2301-f424-e053-dadaa90a57ce	48d8965f-43e6-4160-a06d-a28995fe6e8a
51655-003-52	2026-01-13	C162847	48780-1	9d75b9d1-2301-f424-e053-dadaa90a57ce	48d8965f-43e6-4160-a06d-a28995fe6e8a
51655-003-26	2020-01-31	C162847	48780-1	9d75b9d1-2301-f424-e053-dadaa90a57ce	48d8965f-43e6-4160-a06d-a28995fe6e8a
51655-003-52	2020-01-31	C162847	48780-1	9d75b9d1-2301-f424-e053-dadaa90a57ce	48d8965f-43e6-4160-a06d-a28995fe6e8a

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
BUPROPION HYDROCHLORIDE	ACTIVE INGREDIENT	ZG7E5POY8O	BUPROPION HYDROCHLORIDE ER (BUPROPION HYDROCHLORIDE) TABLET [NORTHWIND PHARMACEUTICALS]	2
BUPROPION	ACTIVE MOIETY	01ZG3TPX31	BUPROPION HYDROCHLORIDE ER (BUPROPION HYDROCHLORIDE) TABLET [NORTHWIND PHARMACEUTICALS]	2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-003	BUPROPION HYDROCHLORIDE ER (BUPROPION HYDROCHLORIDE) TABLET [NORTHWIND PHARMACEUTICALS]	2	Legacy NDC	20141001_48d8965f-43e6-4160-a06d-a28995fe6e8a.zip