Mucus Extended Release

Product NDC
59779-948
11-digit product format
597790948
Labeler code
59779
Product ID
59779-948_abe73e21-79be-4dc0-9faa-93e1c0ff7236
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
CVS Pharmacy
Application
ANDA091009
Marketing category
ANDA
Marketing start
2020-08-11
Marketing end
0000-00-00
Substance
GUAIFENESIN
Active strength
1200 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59779-948-30EA - Each59779-948a201139b-6304-4ead-8bef-dc8057c2dd7812017-03-06
59779-948-55EA - Each59779-948b773828f-109b-4c46-8b04-63188638ae7912017-03-06
59779-948-66EA - Each59779-948facea92f-5818-4767-a86f-1f19eb2c586a12017-03-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59779-948-015977909480128 BLISTER PACK in 1 CARTON (59779-948-01) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK28 blister pack2020-08-110000-00-00NoNoCurrent
59779-948-025977909480242 BLISTER PACK in 1 CARTON (59779-948-02) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK42 blister pack2020-08-130000-00-00NoNoCurrent
59779-948-745977909487414 BLISTER PACK in 1 CARTON (59779-948-74) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK14 blister pack2020-08-110000-00-00NoNoCurrent