tusicof
Generic: dextromethorphan, guaifenesin, and phenylephrine
Labeler: kramer novisDrug Facts
Product Profile
Brand Name
tusicof
Generic Name
dextromethorphan, guaifenesin, and phenylephrine
Labeler
kramer novis
Dosage Form
SYRUP
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/5mL, guaifenesin 400 mg/5mL, phenylephrine hydrochloride 10 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
52083-239
Product ID
52083-239_e954ebb2-df25-40bf-b068-8ac861d6677b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2010-08-17
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52083239
Hyphenated Format
52083-239
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
tusicof (source: ndc)
Generic Name
dextromethorphan, guaifenesin, and phenylephrine (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/5mL
- 400 mg/5mL
- 10 mg/5mL
Packaging
- 30 mL in 1 BOTTLE (52083-239-01)
- 120 mL in 1 BOTTLE (52083-239-04)
- 474 mL in 1 BOTTLE (52083-239-16)
Packages (3)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e954ebb2-df25-40bf-b068-8ac861d6677b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1091331"], "spl_set_id": ["e966b75c-4bb4-4216-8247-baada8f5d759"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Kramer Novis"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (52083-239-01)", "package_ndc": "52083-239-01", "marketing_start_date": "20100817"}, {"sample": false, "description": "120 mL in 1 BOTTLE (52083-239-04)", "package_ndc": "52083-239-04", "marketing_start_date": "20100817"}, {"sample": false, "description": "474 mL in 1 BOTTLE (52083-239-16)", "package_ndc": "52083-239-16", "marketing_start_date": "20121008"}], "brand_name": "TUSICOF", "product_id": "52083-239_e954ebb2-df25-40bf-b068-8ac861d6677b", "dosage_form": "SYRUP", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "52083-239", "generic_name": "dextromethorphan, guaifenesin, and phenylephrine", "labeler_name": "Kramer Novis", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TUSICOF", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100817", "listing_expiration_date": "20261231"}