dextromethorphan hbr. and guaifenesin
Generic: dextromethorphan hbr. and guaifenesin
Labeler: everpharm llcDrug Facts
Product Profile
Brand Name
dextromethorphan hbr. and guaifenesin
Generic Name
dextromethorphan hbr. and guaifenesin
Labeler
everpharm llc
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/10mL, guaifenesin 200 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
84415-011
Product ID
84415-011_2bda25ff-9e45-8f8d-e063-6294a90a6a0f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012.85
Listing Expiration
2026-12-31
Marketing Start
2023-06-12
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84415011
Hyphenated Format
84415-011
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
dextromethorphan hbr. and guaifenesin (source: ndc)
Generic Name
dextromethorphan hbr. and guaifenesin (source: ndc)
Application Number
M012.85 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/10mL
- 200 mg/10mL
Packaging
- 100 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (84415-011-01) / 10 mL in 1 CUP, UNIT-DOSE
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bda25ff-9e45-8f8d-e063-6294a90a6a0f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["996520"], "spl_set_id": ["0c7cd5c4-459d-4e42-ae22-b94f2e29cffb"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Everpharm LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (84415-011-01) / 10 mL in 1 CUP, UNIT-DOSE", "package_ndc": "84415-011-01", "marketing_start_date": "20230612"}], "brand_name": "Dextromethorphan HBr. and Guaifenesin", "product_id": "84415-011_2bda25ff-9e45-8f8d-e063-6294a90a6a0f", "dosage_form": "SOLUTION", "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": "84415-011", "generic_name": "Dextromethorphan HBr. and Guaifenesin", "labeler_name": "Everpharm LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dextromethorphan HBr. and Guaifenesin", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/10mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/10mL"}], "application_number": "M012.85", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230612", "listing_expiration_date": "20261231"}