United States · FDA National Drug Code directory
HYDROMORPHONE HYDROCHLORIDE
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
- 0574-7224_8c369b50-cf2a-4e30-a31c-ccf5f49ab920
- Product NDC
- 0574-7224
- Form
- SUPPOSITORY
- Composition / generic term
- HYDROMORPHONE HYDROCHLORIDE
- Labeler
- Padagis US LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 19960131
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROMORPHONE HYDROCHLORIDE — 3 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 PACKET in 1 BOX (0574-7224-06) / 1 SUPPOSITORY in 1 PACKET · 0574-7224-06
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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