altipres
Generic: dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler: alternative pharmacal corporationDrug Facts
Product Profile
Brand Name
altipres
Generic Name
dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler
alternative pharmacal corporation
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 10 mg/5mL, guaifenesin 200 mg/5mL, phenylephrine hydrochloride 5 mg/5mL
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53163104
Hyphenated Format
53163-104
Supplemental Identifiers
RxCUI
UPC
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
altipres (source: ndc)
Generic Name
dextromethorphan hbr, guaifenesin, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
- 200 mg/5mL
- 5 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (53163-104-16)
Packages (1)
Ingredients (3)
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"}