diabetic tussin dm maximum strength
Generic: dextromethorphan hydrobromide and guaifenesin
Labeler: medtech products incDrug Facts
Product Profile
Brand Name
diabetic tussin dm maximum strength
Generic Name
dextromethorphan hydrobromide and guaifenesin
Labeler
medtech products inc
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/10mL, guaifenesin 400 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
61787-515
Product ID
61787-515_e60166fa-5c2e-4449-9633-97607116cbe5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2020-02-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61787515
Hyphenated Format
61787-515
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
diabetic tussin dm maximum strength (source: ndc)
Generic Name
dextromethorphan hydrobromide and guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/10mL
- 400 mg/10mL
Packaging
- 1 BOTTLE in 1 BOX (61787-515-04) / 118 mL in 1 BOTTLE
- 1 BOTTLE in 1 BOX (61787-515-08) / 237 mL in 1 BOTTLE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e60166fa-5c2e-4449-9633-97607116cbe5", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1046631"], "spl_set_id": ["a10a3b33-7503-4334-8ed7-2bb881df4327"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["MEDTECH PRODUCTS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (61787-515-04) / 118 mL in 1 BOTTLE", "package_ndc": "61787-515-04", "marketing_start_date": "20200201"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (61787-515-08) / 237 mL in 1 BOTTLE", "package_ndc": "61787-515-08", "marketing_start_date": "20200201"}], "brand_name": "Diabetic Tussin DM Maximum Strength", "product_id": "61787-515_e60166fa-5c2e-4449-9633-97607116cbe5", "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": "61787-515", "generic_name": "Dextromethorphan Hydrobromide and Guaifenesin", "labeler_name": "MEDTECH PRODUCTS INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diabetic Tussin DM Maximum Strength", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/10mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/10mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200201", "listing_expiration_date": "20261231"}