DIGOXIN

Product NDC: 66267-443
11-digit product format: 662670443
Labeler code: 66267
Product ID: 66267-443_9cbe6ada-ccb4-6c82-e053-2995a90ab8a5
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: DIGOXIN
Dosage form: TABLET
Route: ORAL
Labeler: NuCare Pharmaceuticals, Inc.
Application: NDA020405
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 2014-01-14
Marketing end: 0000-00-00
Substance: DIGOXIN
Active strength: 0 mg/1
Pharmacologic classes: Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
66267-443-30	2024-08-15	C162847	48780-1	d6a99b39-ed7e-a426-e053-dadaa90af4c2	415b168c-121f-2777-e054-00144ff88e88
66267-443-30	2022-01-28	C162847	48780-1	d6a99b39-ed7e-a426-e053-dadaa90af4c2	415b168c-121f-2777-e054-00144ff88e88

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
66267-443-30	EA - Each	66267-443	1472f5b1-cec7-4a26-9e3a-64a471239a14	1	2017-03-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66267-443-30	66267044330	30 TABLET in 1 BOTTLE (66267-443-30)	30 tablet	2016-11-15	0000-00-00	No	No	Current