United States · FDA National Drug Code directory

Dextromethorphan Polistirex Extended-Release

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
65162-799_9eb36122-c3bf-4b04-84a1-bb137f884c40
Product NDC
65162-799
Form
SUSPENSION
Composition / generic term
Dextromethorphan Polistirex
Labeler
Amneal Pharmaceuticals LLC
Marketing category
ANDA
Marketing start / end (source format)
20170801
Source listing expiry
20261231

Source-listed ingredients

  • DEXTROMETHORPHAN HYDROBROMIDE — 30 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (65162-799-76) / 89 mL in 1 BOTTLE · 65162-799-76
  • 1 BOTTLE in 1 CARTON (65162-799-77) / 148 mL in 1 BOTTLE · 65162-799-77

Source and coverage

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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.

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