mucinex dm

Generic: guaifenesin and dextromethorphan hydrobromide

Labeler: a-s medication solutions
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucinex dm
Generic Name guaifenesin and dextromethorphan hydrobromide
Labeler a-s medication solutions
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1077
Product ID 50090-1077_8c13782f-fcfa-4c99-96f6-8352f0bbfe1a
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA021620
Listing Expiration 2026-12-31
Marketing Start 2012-06-26

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 500901077
Hyphenated Format 50090-1077

Supplemental Identifiers

RxCUI
1298324
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

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 mucinex dm (source: ndc)
Generic Name guaifenesin and dextromethorphan hydrobromide (source: ndc)
Application Number NDA021620 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
  • 600 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-1077-0) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

50090-1077-0 1 BLISTER PACK in 1 CARTON (50090-1077-0) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

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

Linked Drug Pages (1)

MUCINEX DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8c13782f-fcfa-4c99-96f6-8352f0bbfe1a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["fcaf1df9-b396-44f2-94ce-e46e80aba66c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-1077-0)  / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "50090-1077-0", "marketing_start_date": "20141128"}], "brand_name": "MUCINEX DM", "product_id": "50090-1077_8c13782f-fcfa-4c99-96f6-8352f0bbfe1a", "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": "50090-1077", "generic_name": "Guaifenesin and Dextromethorphan Hydrobromide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCINEX DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "NDA021620", "marketing_category": "NDA", "marketing_start_date": "20120626", "listing_expiration_date": "20261231"}