tussin cough expectorant cough supressant dm
Generic: dextromethorphan hydrobromide
Labeler: aptapharma inc.Drug Facts
Product Profile
Brand Name
tussin cough expectorant cough supressant dm
Generic Name
dextromethorphan hydrobromide
Labeler
aptapharma inc.
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 10 mg/5mL, guaifenesin 100 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
76281-503
Product ID
76281-503_5b440237-78c8-458a-b365-8b77ae10fdd3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2020-09-30
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76281503
Hyphenated Format
76281-503
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
tussin cough expectorant cough supressant dm (source: ndc)
Generic Name
dextromethorphan hydrobromide (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
- 100 mg/5mL
Packaging
- 118 mL in 1 BOTTLE (76281-503-24)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5b440237-78c8-458a-b365-8b77ae10fdd3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["996520"], "spl_set_id": ["8a4c55d0-c472-4e89-9fdb-17ecf0af4856"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["AptaPharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (76281-503-24)", "package_ndc": "76281-503-24", "marketing_start_date": "20200930"}], "brand_name": "TUSSIN COUGH EXPECTORANT COUGH SUPRESSANT DM", "product_id": "76281-503_5b440237-78c8-458a-b365-8b77ae10fdd3", "dosage_form": "LIQUID", "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": "76281-503", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE", "labeler_name": "AptaPharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TUSSIN COUGH", "brand_name_suffix": "EXPECTORANT COUGH SUPRESSANT DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200930", "listing_expiration_date": "20261231"}