triponel

Generic: dextromethorphan hbr, phenylephrine hcl, triprolidine hcl

Labeler: llorens pharmaceuticals international division
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name triponel
Generic Name dextromethorphan hbr, phenylephrine hcl, triprolidine hcl
Labeler llorens pharmaceuticals international division
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 15 mg/5mL, phenylephrine hydrochloride 5 mg/5mL, triprolidine hydrochloride 1.25 mg/5mL

Manufacturer
LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION

Identifiers & Regulatory

Product NDC 54859-508
Product ID 54859-508_47461d04-60e6-bfde-e063-6394a90aaeec
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2019-08-01

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] 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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 54859508
Hyphenated Format 54859-508

Supplemental Identifiers

RxCUI
2268058
UNII
9D2RTI9KYH 04JA59TNSJ YAN7R5L890

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 triponel (source: ndc)
Generic Name dextromethorphan hbr, phenylephrine hcl, triprolidine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/5mL
  • 5 mg/5mL
  • 1.25 mg/5mL
source: ndc
Packaging
  • 474 mL in 1 BOTTLE (54859-508-16)
source: ndc

Packages (1)

Ingredients (3)

dextromethorphan hydrobromide (15 mg/5mL) phenylephrine hydrochloride (5 mg/5mL) triprolidine hydrochloride (1.25 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47461d04-60e6-bfde-e063-6394a90aaeec", "openfda": {"unii": ["9D2RTI9KYH", "04JA59TNSJ", "YAN7R5L890"], "rxcui": ["2268058"], "spl_set_id": ["cc774d33-96ce-4992-ad30-3cb03b0d119d"], "manufacturer_name": ["LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "474 mL in 1 BOTTLE (54859-508-16)", "package_ndc": "54859-508-16", "marketing_start_date": "20190801"}], "brand_name": "Triponel", "product_id": "54859-508_47461d04-60e6-bfde-e063-6394a90aaeec", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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": "54859-508", "generic_name": "Dextromethorphan HBr, Phenylephrine HCl, Triprolidine HCl", "labeler_name": "LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Triponel", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/5mL"}, {"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "1.25 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}