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
- 63304-758_4d15b836-54c7-2f40-e063-6294a90a68a2
- Product NDC
- 63304-758
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- morphine sulfate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120511
- Source listing expiry
- 20271231
Source-listed ingredients
- MORPHINE SULFATE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-01) · 63304-758-01
- 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-03) · 63304-758-03
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-05) · 63304-758-05
- 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-50) · 63304-758-50
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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