Health Mart mucus relief d

Product NDC
62011-0259
11-digit product format
620110259
Labeler code
62011
Product ID
62011-0259_22a6c2c4-b1bf-41fc-99a9-d1b51c57926f
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin, pseudoephedrine hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Strategic Sourcing Services LLC
Application
ANDA091071
Marketing category
ANDA
Marketing start
2015-12-21
Marketing end
0000-00-00
Substance
GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Active strength
600 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62011-0259-1EA - Each62011-0259e7a316e0-852c-4a2e-bf59-c36c32774a2f12016-04-04

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62011-0259-16201102590118 BLISTER PACK in 1 CARTON (62011-0259-1) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK18 blister pack2015-12-210000-00-00NoNoCurrent