Mucus Relief DM

Product NDC
69256-733
11-digit product format
692560733
Labeler code
69256
Product ID
69256-733_4677c8a9-6c58-4bfb-9b6c-44ffedd98fb0
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin, Dextromethorphan HBr
Dosage form
TABLET
Route
ORAL
Labeler
Harris Teeter, LLC
Application
ANDA209692
Marketing category
ANDA
Marketing start
2021-05-28
Marketing end
2026-05-28
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
30; 600 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
Current FDA listing
Yes

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69256-733MUCUS RELIEF DM (GUAIFENESIN, DEXTROMETHORPHAN HBR) TABLET [HARRIS TEETER, LLC]3Current NDC, Legacy NDC20250306_c5752a62-3258-499b-a92f-51331dc1108d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69256-733-206925607332020 BLISTER PACK in 1 CARTON (69256-733-20) / 1 TABLET in 1 BLISTER PACK20 blister pack2021-05-282026-05-28NoNoCurrent