mucus relief dm maximum strength (21130-989)

Drug Facts

Product Profile

Brand Name mucus relief dm maximum strength

Generic Name guaifenesin and dextromethorphan hbr

Labeler better living brands llc

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

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

Manufacturer

Better Living Brands LLC

Identifiers & Regulatory

Product NDC 21130-989

Product ID 21130-989_91782655-a29b-4bda-b514-5489279b3edb

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA206941

Listing Expiration 2026-12-31

Marketing Start 2017-03-17

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 21130989

Hyphenated Format 21130-989

Supplemental Identifiers

RxCUI

1099074

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 and dextromethorphan hbr (source: ndc)

Application Number ANDA206941 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

60 mg/1
1200 mg/1

source: ndc

Packaging

4 BLISTER PACK in 1 CARTON (21130-989-03) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
2 BLISTER PACK in 1 CARTON (21130-989-65) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (2)

21130-989-03 4 BLISTER PACK in 1 CARTON (21130-989-03) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 21130-989-65 2 BLISTER PACK in 1 CARTON (21130-989-65) / 7 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 MAXIMUM STRENGTH ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "91782655-a29b-4bda-b514-5489279b3edb", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["4ee69f46-3dc6-4249-9b04-186fa0a13e84"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Better Living Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (21130-989-03)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "21130-989-03", "marketing_start_date": "20220428"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (21130-989-65)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "21130-989-65", "marketing_start_date": "20170317"}], "brand_name": "Mucus Relief DM MAXIMUM STRENGTH", "product_id": "21130-989_91782655-a29b-4bda-b514-5489279b3edb", "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": "21130-989", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Better Living Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM MAXIMUM STRENGTH", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20170317", "listing_expiration_date": "20261231"}