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
- 63629-4284_f895b5fa-f576-4ee7-9747-ada5688ca1ab
- Product NDC
- 63629-4284
- Form
- TABLET
- Composition / generic term
- Hydromorphone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20091123
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROMORPHONE HYDROCHLORIDE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 25 TABLET in 1 BOTTLE (63629-4284-1) · 63629-4284-1
- 60 TABLET in 1 BOTTLE (63629-4284-2) · 63629-4284-2
- 30 TABLET in 1 BOTTLE (63629-4284-3) · 63629-4284-3
- 28 TABLET in 1 BOTTLE (63629-4284-4) · 63629-4284-4
- 90 TABLET in 1 BOTTLE (63629-4284-5) · 63629-4284-5
- 120 TABLET in 1 BOTTLE (63629-4284-6) · 63629-4284-6
- 40 TABLET in 1 BOTTLE (63629-4284-7) · 63629-4284-7
- 20 TABLET in 1 BOTTLE (63629-4284-8) · 63629-4284-8
- 10 TABLET in 1 BOTTLE (63629-4284-9) · 63629-4284-9
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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