mucus relief dm (59726-840)

Drug Facts

Product Profile

Brand Name mucus relief dm

Generic Name guaifenesin, dextromethorphan hbr

Labeler p & l development, llc

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1

Manufacturer

P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-840

Product ID 59726-840_16ad157b-f9b4-455c-a9ca-da2da3c401dc

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA209692

Listing Expiration 2027-12-31

Marketing Start 2026-02-05

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 59726840

Hyphenated Format 59726-840

Supplemental Identifiers

RxCUI

1099074

UPC

0359726734172

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 guaifenesin, dextromethorphan hbr (source: ndc)

Application Number ANDA209692 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

60 mg/1
1200 mg/1

source: ndc

Packaging

14 BLISTER PACK in 1 CARTON (59726-840-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (1)

59726-840-14 14 BLISTER PACK in 1 CARTON (59726-840-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

dextromethorphan hydrobromide (60 mg/1) guaifenesin (1200 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": "16ad157b-f9b4-455c-a9ca-da2da3c401dc", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0359726734172"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["3586b3f0-55eb-489c-ab6f-26c39d0910de"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (59726-840-14)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "59726-840-14", "marketing_start_date": "20260301"}], "brand_name": "Mucus Relief DM", "product_id": "59726-840_16ad157b-f9b4-455c-a9ca-da2da3c401dc", "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": "59726-840", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA209692", "marketing_category": "ANDA", "marketing_start_date": "20260205", "listing_expiration_date": "20271231"}