Metoprolol Succinate

Product NDC: 51655-580
11-digit product format: 516550580
Labeler code: 51655
Product ID: 51655-580_29d4a7fc-d528-41c5-b180-3bef81100879
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Metoprolol Succinate
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA076862
Marketing category: ANDA
Marketing start: 2014-05-07
Marketing end: 0000-00-00
Substance: METOPROLOL SUCCINATE
Active strength: 50 mg/301
Pharmacologic classes: Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
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
51655-580-52	2026-01-08	C162847	48780-1	9d75b9d1-2b4d-f424-e053-dadaa90a57ce	4df476ac-6794-4435-833f-5e341f4585d7
51655-580-52	2020-01-31	C162847	48780-1	9d75b9d1-2b4d-f424-e053-dadaa90a57ce	4df476ac-6794-4435-833f-5e341f4585d7

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
METOPROLOL SUCCINATE	ACTIVE INGREDIENT	TH25PD4CCB	METOPROLOL SUCCINATE TABLET, FILM COATED, EXTENDED RELEASE [NORTHWIND PHARMACEUTICALS]	1
METOPROLOL	ACTIVE MOIETY	GEB06NHM23	METOPROLOL SUCCINATE TABLET, FILM COATED, EXTENDED RELEASE [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-580	METOPROLOL SUCCINATE TABLET, FILM COATED, EXTENDED RELEASE [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20140520_4df476ac-6794-4435-833f-5e341f4585d7.zip