Mucus Relief DM Extended Release

Product NDC
11673-833
11-digit product format
116730833
Labeler code
11673
Product ID
11673-833_7f9325ab-5936-4883-b649-9748009f287f
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin, Dextromethorphan HBr
Dosage form
TABLET
Route
ORAL
Labeler
TARGET Corporation
Application
ANDA209692
Marketing category
ANDA
Marketing start
2019-01-01
Marketing end
2025-05-30
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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-833MUCUS RELIEF DM EXTENDED RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR) TABLET [TARGET CORPORATION]4Legacy NDC20221118_e18db792-3f9b-4ae2-b27e-c15c3bf14fef.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-833-201167308332020 BLISTER PACK in 1 CARTON (11673-833-20) > 1 TABLET in 1 BLISTER PACK20 blister pack2019-01-012025-05-30NoNoCurrent
11673-833-401167308334040 BLISTER PACK in 1 CARTON (11673-833-40) > 1 TABLET in 1 BLISTER PACK40 blister pack2019-01-012025-05-30NoNoCurrent