mucus dm extended release
Generic: guaifenesin and dextromethorphan hbr
Labeler: cvs pharmacy, inc.Drug Facts
Product Profile
Brand Name
mucus dm extended release
Generic Name
guaifenesin and dextromethorphan hbr
Labeler
cvs pharmacy, inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69842-057
Product ID
69842-057_b793ab0a-5809-46d0-b57a-7ad03b29f959
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842057
Hyphenated Format
69842-057
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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 and dextromethorphan hbr (source: ndc)
Application Number
ANDA206941 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
- 600 mg/1
Packaging
- 4 BLISTER PACK in 1 CARTON (69842-057-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (69842-057-67) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b793ab0a-5809-46d0-b57a-7ad03b29f959", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["2aa1889f-bb76-4e70-81b5-c25c4ebab113"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (69842-057-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "69842-057-11", "marketing_start_date": "20170317"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (69842-057-67) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "69842-057-67", "marketing_start_date": "20170317"}], "brand_name": "Mucus DM Extended Release", "product_id": "69842-057_b793ab0a-5809-46d0-b57a-7ad03b29f959", "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": "69842-057", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "CVS Pharmacy, Inc.", "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": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20170317", "listing_expiration_date": "20261231"}