dextromethorphan hbr. and guaifenesin
Generic: dextromethorphan hbr. and guaifenesin
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
dextromethorphan hbr. and guaifenesin
Generic Name
dextromethorphan hbr. and guaifenesin
Labeler
rising pharma holdings, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/10mL, guaifenesin 200 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
57237-313
Product ID
57237-313_914d13bb-fbd6-420f-ad2c-1df3828d18c3
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
57237313
Hyphenated Format
57237-313
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
- 80 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (57237-313-18) / 10 mL in 1 CUP, UNIT-DOSE (57237-313-01)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "914d13bb-fbd6-420f-ad2c-1df3828d18c3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["996520"], "spl_set_id": ["e463e60f-d0db-4ee7-9713-ddf25aa38a43"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (57237-313-18) / 10 mL in 1 CUP, UNIT-DOSE (57237-313-01)", "package_ndc": "57237-313-18", "marketing_start_date": "20230612"}], "brand_name": "Dextromethorphan HBr. and Guaifenesin", "product_id": "57237-313_914d13bb-fbd6-420f-ad2c-1df3828d18c3", "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": "57237-313", "generic_name": "Dextromethorphan HBr. and Guaifenesin", "labeler_name": "Rising Pharma Holdings, Inc.", "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"}