Carvedilol

Product NDC: 51655-002
11-digit product format: 516550002
Labeler code: 51655
Product ID: 51655-002_b6948d4a-cf4b-4e3a-918b-d6faef6ac0c7
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Carvedilol
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA077316
Marketing category: ANDA
Marketing start: 2014-05-16
Marketing end: 0000-00-00
Substance: CARVEDILOL
Active strength: 13 mg/301
Pharmacologic classes: Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],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
51655-002-52	2026-01-13	C162847	48780-1	9d75b9d0-4fc3-f424-e053-dadaa90a57ce	b93697b3-c328-41b4-a012-13417bcc5169
51655-002-52	2020-01-31	C162847	48780-1	9d75b9d0-4fc3-f424-e053-dadaa90a57ce	b93697b3-c328-41b4-a012-13417bcc5169

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
CARVEDILOL	ACTIVE INGREDIENT	0K47UL67F2	CARVEDILOL TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1
CARVEDILOL	ACTIVE MOIETY	0K47UL67F2	CARVEDILOL TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-002	CARVEDILOL TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20140516_b93697b3-c328-41b4-a012-13417bcc5169.zip