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
- 71335-0723_dd7057dd-4448-4f11-8c2d-6a1bfe0e1f50
- Product NDC
- 71335-0723
- Form
- TABLET
- Composition / generic term
- HYDROMORPHONE HYDROCHLORIDE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160517
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROMORPHONE HYDROCHLORIDE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (71335-0723-0) · 71335-0723-0
- 30 TABLET in 1 BOTTLE (71335-0723-1) · 71335-0723-1
- 180 TABLET in 1 BOTTLE (71335-0723-2) · 71335-0723-2
- 120 TABLET in 1 BOTTLE (71335-0723-3) · 71335-0723-3
- 20 TABLET in 1 BOTTLE (71335-0723-4) · 71335-0723-4
- 25 TABLET in 1 BOTTLE (71335-0723-5) · 71335-0723-5
- 100 TABLET in 1 BOTTLE (71335-0723-6) · 71335-0723-6
- 60 TABLET in 1 BOTTLE (71335-0723-7) · 71335-0723-7
- 56 TABLET in 1 BOTTLE (71335-0723-8) · 71335-0723-8
- 140 TABLET in 1 BOTTLE (71335-0723-9) · 71335-0723-9
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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