Maximum Strength Mucus Relief

Product NDC: 46122-583
11-digit product format: 461220583
Labeler code: 46122
Product ID: 46122-583_530c8ce6-676d-4a98-b9c1-5cf6f67abf9d
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin
Dosage form: TABLET, EXTENDED RELEASE
Route: ORAL
Labeler: Amerisource Bergen
Application: ANDA209215
Marketing category: ANDA
Marketing start: 2019-11-01
Marketing end: 0000-00-00
Substance: GUAIFENESIN
Active strength: 1200 mg/1
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
46122-583-74	2024-06-28	C162847	48780-1	1030e365-42e4-111a-e063-dadaa90a10e2	8679de8f-a4cb-4dc6-9fac-f8e378dba3f9
46122-583-74	2024-01-30	C162847	48780-1	1030e365-42e4-111a-e063-dadaa90a10e2	8679de8f-a4cb-4dc6-9fac-f8e378dba3f9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
46122-583-74	EA - Each	46122-583	30797659-8502-4b44-aa42-e9de8ae1e5eb	1	2022-07-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
46122-583-74	46122058374	2 BLISTER PACK in 1 CARTON (46122-583-74) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK	2 blister pack	2019-11-01	0000-00-00	No	No	Current