Mucus Relief DM Extended Release Caplets

Product NDC
37012-730
11-digit product format
370120730
Labeler code
37012
Product ID
37012-730_cd817d2f-ccde-4734-a1af-f60b748036ca
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin, Dextromethorphan HBr
Dosage form
TABLET
Route
ORAL
Labeler
Shopko Stores Operating Co., LLC.
Application
ANDA209692
Marketing category
ANDA
Marketing start
2019-01-04
Marketing end
2022-12-30
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
30 mg/1; mg/1
Pharmacologic classes
Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37012-730-203701207302020 BLISTER PACK in 1 CARTON (37012-730-20) > 1 TABLET in 1 BLISTER PACK20 blister pack2019-01-042022-12-30NoNoCurrent
37012-730-403701207304040 BLISTER PACK in 1 CARTON (37012-730-40) > 1 TABLET in 1 BLISTER PACK40 blister pack2019-01-042022-12-30NoNoCurrent