mucinex dm
Generic: guaifenesin and dextromethorphan hydrobromide
Labeler: lil' drug store products, inc.Drug Facts
Product Profile
Brand Name
mucinex dm
Generic Name
guaifenesin and dextromethorphan hydrobromide
Labeler
lil' drug store products, inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
66715-9724
Product ID
66715-9724_075d4215-dba2-3d49-e063-6394a90a1e25
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA021620
Listing Expiration
2026-12-31
Marketing Start
2010-05-10
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
667159724
Hyphenated Format
66715-9724
Supplemental Identifiers
RxCUI
UPC
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
mucinex dm (source: ndc)
Generic Name
guaifenesin and dextromethorphan hydrobromide (source: ndc)
Application Number
NDA021620 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
- 600 mg/1
Packaging
- 1 POUCH in 1 CARTON (66715-9724-1) / 2 TABLET, EXTENDED RELEASE in 1 POUCH
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "075d4215-dba2-3d49-e063-6394a90a1e25", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0761706164211"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["c274b05c-8f05-4980-9a93-77affb322e57"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Lil' Drug Store Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (66715-9724-1) / 2 TABLET, EXTENDED RELEASE in 1 POUCH", "package_ndc": "66715-9724-1", "marketing_start_date": "20100510"}], "brand_name": "Mucinex DM", "product_id": "66715-9724_075d4215-dba2-3d49-e063-6394a90a1e25", "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": "66715-9724", "generic_name": "Guaifenesin and Dextromethorphan Hydrobromide", "labeler_name": "Lil' Drug Store Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "NDA021620", "marketing_category": "NDA", "marketing_start_date": "20100510", "listing_expiration_date": "20261231"}