mucus relief dm (70677-1049)

Drug Facts

Product Profile

Brand Name mucus relief dm

Generic Name guaifenesin, dextromethorphan hbr

Labeler strategic sourcing services llc

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

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

Manufacturer

Strategic Sourcing Services LLC

Identifiers & Regulatory

Product NDC 70677-1049

Product ID 70677-1049_cd619d8c-2e04-46b4-99d7-ab2563380e38

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA209692

Listing Expiration 2026-12-31

Marketing Start 2023-03-01

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 706771049

Hyphenated Format 70677-1049

Supplemental Identifiers

RxCUI

1099074

UPC

0010939955708

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 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 (70677-1049-1) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (1)

70677-1049-1 14 BLISTER PACK in 1 CARTON (70677-1049-1) / 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": "cd619d8c-2e04-46b4-99d7-ab2563380e38", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0010939955708"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["5eb5f84f-4cb8-4552-b73d-c2b27657fa15"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Strategic Sourcing Services LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (70677-1049-1)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "70677-1049-1", "marketing_start_date": "20230301"}], "brand_name": "Mucus Relief DM", "product_id": "70677-1049_cd619d8c-2e04-46b4-99d7-ab2563380e38", "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": "70677-1049", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "Strategic Sourcing Services 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": "20230301", "listing_expiration_date": "20261231"}