mucus relief dm maximum strength (68016-674)

Drug Facts

Product Profile

Brand Name mucus relief dm maximum strength

Generic Name guaifenesin, dextromethorphan hbr

Labeler chain drug consortium, llc

Dosage Form TABLET

Routes

ORAL

Active Ingredients

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

Manufacturer

Chain Drug Consortium, LLC

Identifiers & Regulatory

Product NDC 68016-674

Product ID 68016-674_1730a5b2-b308-4dfb-813c-0536d0b91ea3

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA209692

Marketing Start 2019-11-29

Marketing End 2026-12-31

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 68016674

Hyphenated Format 68016-674

Supplemental Identifiers

RxCUI

1099074

UPC

0840986036675

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 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 (68016-674-14) / 1 TABLET in 1 BLISTER PACK
28 BLISTER PACK in 1 CARTON (68016-674-28) / 1 TABLET in 1 BLISTER PACK

source: ndc

Packages (2)

68016-674-14 14 BLISTER PACK in 1 CARTON (68016-674-14) / 1 TABLET in 1 BLISTER PACK 68016-674-28 28 BLISTER PACK in 1 CARTON (68016-674-28) / 1 TABLET in 1 BLISTER PACK

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": "1730a5b2-b308-4dfb-813c-0536d0b91ea3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0840986036675"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["d6aae1a1-0ab9-4b26-9f62-b8761014bb35"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (68016-674-14)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "68016-674-14", "marketing_end_date": "20261231", "marketing_start_date": "20191129"}, {"sample": false, "description": "28 BLISTER PACK in 1 CARTON (68016-674-28)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "68016-674-28", "marketing_end_date": "20261231", "marketing_start_date": "20191129"}], "brand_name": "Mucus Relief DM Maximum Strength", "product_id": "68016-674_1730a5b2-b308-4dfb-813c-0536d0b91ea3", "dosage_form": "TABLET", "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": "68016-674", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "Chain Drug Consortium, LLC", "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": "ANDA209692", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20191129"}