mucus relief - dm maximum strength

Generic: guaifenesin, dextromethorphan hbr

Labeler: yyba corp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief - dm maximum strength
Generic Name guaifenesin, dextromethorphan hbr
Labeler yyba corp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
YYBA CORP

Identifiers & Regulatory

Product NDC 73581-405
Product ID 73581-405_3ce33efd-e300-a7e2-e063-6394a90ad2c1
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA214781
Listing Expiration 2026-12-31
Marketing Start 2025-04-01

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 73581405
Hyphenated Format 73581-405

Supplemental Identifiers

RxCUI
1099074
UPC
0373581000715
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 maximum strength (source: ndc)
Generic Name guaifenesin, dextromethorphan hbr (source: ndc)
Application Number ANDA214781 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 1200 mg/1
source: ndc
Packaging
  • 98 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (73581-405-98)
source: ndc

Packages (1)

73581-405-98 98 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (73581-405-98)

Ingredients (2)

dextromethorphan hydrobromide (60 mg/1) guaifenesin (1200 mg/1)

Linked Drug Pages (1)

MUCUS RELIEF - DM MAXIMUM STRENGTH ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ce33efd-e300-a7e2-e063-6394a90ad2c1", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0373581000715"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["325b5e55-ba58-312c-e063-6394a90aee55"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["YYBA CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "98 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (73581-405-98)", "package_ndc": "73581-405-98", "marketing_start_date": "20250401"}], "brand_name": "MUCUS RELIEF - DM MAXIMUM STRENGTH", "product_id": "73581-405_3ce33efd-e300-a7e2-e063-6394a90ad2c1", "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": "73581-405", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "YYBA CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCUS RELIEF - DM", "brand_name_suffix": "MAXIMUM STRENGTH", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA214781", "marketing_category": "ANDA", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}