altipres

Generic: dextromethorphan hbr, guaifenesin, phenylephrine hcl

Labeler: alternative pharmacal corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name altipres
Generic Name dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler alternative pharmacal corporation
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 10 mg/5mL, guaifenesin 200 mg/5mL, phenylephrine hydrochloride 5 mg/5mL

Manufacturer
Alternative Pharmacal Corporation

Identifiers & Regulatory

Product NDC 53163-104
Product ID 53163-104_472ecc1a-795d-b592-e063-6394a90a1bb2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2013-05-01

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 53163104
Hyphenated Format 53163-104

Supplemental Identifiers

RxCUI
1098647
UPC
0353163104161
UNII
9D2RTI9KYH 495W7451VQ 04JA59TNSJ
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 altipres (source: ndc)
Generic Name dextromethorphan hbr, guaifenesin, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/5mL
  • 200 mg/5mL
  • 5 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (53163-104-16)
source: ndc

Packages (1)

Ingredients (3)

dextromethorphan hydrobromide (10 mg/5mL) guaifenesin (200 mg/5mL) phenylephrine hydrochloride (5 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "472ecc1a-795d-b592-e063-6394a90a1bb2", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0353163104161"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1098647"], "spl_set_id": ["c5a43107-3eb8-46bb-87bd-20deafe28c3f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Alternative Pharmacal Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (53163-104-16)", "package_ndc": "53163-104-16", "marketing_start_date": "20130501"}], "brand_name": "Altipres", "product_id": "53163-104_472ecc1a-795d-b592-e063-6394a90a1bb2", "dosage_form": "LIQUID", "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": "53163-104", "generic_name": "Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl", "labeler_name": "Alternative Pharmacal Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Altipres", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130501", "listing_expiration_date": "20261231"}