mucus relief dm (41250-436)

Drug Facts

Product Profile

Brand Name mucus relief dm

Generic Name dextromethorphan hydrobromide, guaifenesin

Labeler meijer distribution inc

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1

Manufacturer

Meijer Distribution Inc

Identifiers & Regulatory

Product NDC 41250-436

Product ID 41250-436_72597fb2-a000-47ad-9672-392c5db34c44

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA207602

Listing Expiration 2026-12-31

Marketing Start 2020-06-02

Pharmacologic Class

Established (EPC)

expectorant [epc]

Physiologic Effect

decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 41250436

Hyphenated Format 41250-436

Supplemental Identifiers

RxCUI

1298324

UNII

9D2RTI9KYH 495W7451VQ

NUI

N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name mucus relief dm (source: ndc)

Generic Name dextromethorphan hydrobromide, guaifenesin (source: ndc)

Application Number ANDA207602 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

30 mg/1
600 mg/1

source: ndc

Packaging

1 BOTTLE in 1 CARTON (41250-436-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
1 BOTTLE in 1 CARTON (41250-436-49) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE

source: ndc

Packages (2)

41250-436-01 1 BOTTLE in 1 CARTON (41250-436-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE 41250-436-49 1 BOTTLE in 1 CARTON (41250-436-49) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE

Ingredients (2)

dextromethorphan hydrobromide (30 mg/1) guaifenesin (600 mg/1)

Linked Drug Pages (1)

mucus relief dm ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "72597fb2-a000-47ad-9672-392c5db34c44", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["d41749b4-735b-44f7-ab06-244f68e031e3"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-436-01)  / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "41250-436-01", "marketing_start_date": "20200602"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-436-49)  / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "41250-436-49", "marketing_start_date": "20200602"}], "brand_name": "mucus relief dm", "product_id": "41250-436_72597fb2-a000-47ad-9672-392c5db34c44", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_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 Antagonists [MoA]"], "product_ndc": "41250-436", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "mucus relief dm", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA207602", "marketing_category": "ANDA", "marketing_start_date": "20200602", "listing_expiration_date": "20261231"}