United States · FDA National Drug Code directory
Altipres Pediatric
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 45737-105_472eca54-1c0a-770e-e063-6294a90a7e01
- Product NDC
- 45737-105
- Form
- LIQUID
- Composition / generic term
- Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
- Labeler
- Advanced Generic Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20241201
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROMETHORPHAN HYDROBROMIDE — 5 mg/5mL
- GUAIFENESIN — 75 mg/5mL
- PHENYLEPHRINE HYDROCHLORIDE — 2.5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (45737-105-16) · 45737-105-16
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →