MUCINEX

Product NDC: 61919-651
11-digit product format: 619190651
Labeler code: 61919
Product ID: 61919-651_9ca985c6-5018-0558-e053-2995a90a8202
Type: HUMAN OTC DRUG
Nonproprietary name: MUCINEX
Dosage form: TABLET, EXTENDED RELEASE
Route: ORAL
Labeler: DIRECT RX
Application: NDA021282
Marketing category: NDA
Marketing start: 2014-01-01
Marketing end: 0000-00-00
Substance: GUAIFENESIN
Active strength: 600 mg/1
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
61919-651-20	2023-10-06	C162847	48780-1	f386c649-d282-0266-e053-dadaa90a7c1a	615ac5b7-426c-4bfb-9826-87735c6288cb
61919-651-20	2023-01-30	C162847	48780-1	f386c649-d282-0266-e053-dadaa90a7c1a	615ac5b7-426c-4bfb-9826-87735c6288cb

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
61919-651-20	EA - Each	61919-651	13aea766-82fa-4c45-ba43-0f22ddfcf54f	1	2015-04-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
61919-651-20	61919065120	20 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-651-20)	2015-01-01	0000-00-00	No	No	Current