United States · FDA National Drug Code directory

Dilaudid

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
42858-338_3348b431-907c-4f1d-8a18-e4be2a04df23
Product NDC
42858-338
Form
TABLET
Composition / generic term
hydromorphone hydrochloride
Labeler
Rhodes Pharmaceuticals LLC
Marketing category
NDA
Marketing start / end (source format)
20170515
Source listing expiry
20271231

Source-listed ingredients

  • HYDROMORPHONE HYDROCHLORIDE — 8 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE, PLASTIC (42858-338-01) · 42858-338-01

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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