mucus dm extended release (69842-963)

Drug Facts

Product Profile

Brand Name mucus dm extended release

Generic Name guaifenesin, dextromethorphan hydrobromide

Labeler cvs pharmacy

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

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

Manufacturer

CVS Pharmacy

Identifiers & Regulatory

Product NDC 69842-963

Product ID 69842-963_e6de3982-4439-4272-9d2c-60d88236f877

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA207602

Listing Expiration 2026-12-31

Marketing Start 2019-09-13

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 69842963

Hyphenated Format 69842-963

Supplemental Identifiers

RxCUI

1298324

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 dm extended release (source: ndc)

Generic Name guaifenesin, dextromethorphan hydrobromide (source: ndc)

Application Number ANDA207602 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

30 mg/1
600 mg/1

source: ndc

Packaging

1 BOTTLE in 1 CARTON (69842-963-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE

source: ndc

Packages (1)

69842-963-01 1 BOTTLE in 1 CARTON (69842-963-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

mucus dm extended release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "e6de3982-4439-4272-9d2c-60d88236f877", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["6c9540ae-aea1-4717-8dca-60850ebdb1b4"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-963-01)  / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "69842-963-01", "marketing_start_date": "20190913"}], "brand_name": "mucus dm extended release", "product_id": "69842-963_e6de3982-4439-4272-9d2c-60d88236f877", "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": "69842-963", "generic_name": "guaifenesin, dextromethorphan hydrobromide", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "mucus dm extended release", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA207602", "marketing_category": "ANDA", "marketing_start_date": "20190913", "listing_expiration_date": "20261231"}