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Product NDC
49035-729
11-digit product format
490350729
Labeler code
49035
Product ID
49035-729_1667b36a-fe06-4992-9cf9-f68176eaf201
Type
HUMAN OTC DRUG
Nonproprietary name
guaifenesin, pseudoephedrine hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Wal-Mart Stores Inc
Application
ANDA091071
Marketing category
ANDA
Marketing start
2020-07-24
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-729-684903507296836 BLISTER PACK in 1 CARTON (49035-729-68) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK36 blister pack2020-07-240000-00-00NoNoCurrent
49035-729-894903507298918 BLISTER PACK in 1 CARTON (49035-729-89) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK18 blister pack2020-07-240000-00-00NoNoCurrent