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NDC 41250-0633-40 Mucus Relief DM Extended Release Caplets 30; 600 mg/1; mg/1 Details

Mucus Relief DM Extended Release Caplets 30; 600 mg/1; mg/1

Mucus Relief DM Extended Release Caplets is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by MEIJER, INC.. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.

MedlinePlus Drug Summary

Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.

Related Packages: 41250-0633-40
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Dextromethorphan

Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.

Related Packages: 41250-0633-40
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Guaifenesin

Product Information

NDC	41250-0633
Product ID	41250-633_69443323-d4c7-43a6-a976-f897e883ef6b
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Mucus Relief DM Extended Release Caplets
Proprietary Name Suffix	n/a
Non-Proprietary Name	Guaifenesin, Dextromethorphan HBr
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	30; 600
Active Ingredient Units	mg/1; mg/1
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Labeler Name	MEIJER, INC.
Pharmaceutical Class	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 Ant
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA209692
Listing Certified Through	n/a

Package

NDC 41250-0633-40 (41250063340)

Pricing Information	N/A
NDC Package Code	41250-633-40
Billing NDC	41250063340
Package	40 BLISTER PACK in 1 CARTON (41250-633-40) / 1 TABLET in 1 BLISTER PACK
Marketing Start Date	2019-11-01
NDC Exclude Flag	N