diabetic tussin dm maximum strength

Generic: dextromethorphan hydrobromide and guaifenesin

Labeler: medtech products inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name diabetic tussin dm maximum strength
Generic Name dextromethorphan hydrobromide and guaifenesin
Labeler medtech products inc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 20 mg/10mL, guaifenesin 400 mg/10mL

Manufacturer
MEDTECH PRODUCTS INC

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)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61787515
Hyphenated Format 61787-515

Supplemental Identifiers

RxCUI
1046631
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/10mL
  • 400 mg/10mL
source: ndc
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
source: ndc

Packages (2)

Ingredients (2)

dextromethorphan hydrobromide (20 mg/10mL) guaifenesin (400 mg/10mL)

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"}