United States · FDA National Drug Code directory
Sanaflu Xtra
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
- 48201-001_42404180-fa1a-fcf6-e063-6394a90a281f
- Product NDC
- 48201-001
- Form
- CAPSULE, GELATIN COATED
- Composition / generic term
- ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
- Labeler
- GRANDALL DISTRIBUTING, LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20150430
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROMETHORPHAN HYDROBROMIDE — 10 mg/1
- PHENYLEPHRINE HYDROCHLORIDE — 5 mg/1
- ACETAMINOPHEN — 250 mg/1
- CHLORPHENIRAMINE MALEATE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 CAPSULE, GELATIN COATED in 1 BOX (48201-001-12) · 48201-001-12
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 →