United States · FDA National Drug Code directory
Morphine sulfate
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
- 72162-1791_0c6a93c2-80bb-47dc-9a64-717724b23302
- Product NDC
- 72162-1791
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- morphine sulfate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120511 / 20261231
Source-listed ingredients
- MORPHINE SULFATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-1) · 72162-1791-1
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-3) · 72162-1791-3
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-6) · 72162-1791-6
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-9) · 72162-1791-9
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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