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
- 71335-0707_1232954b-d43d-4060-8876-86e38a14f8d9
- Product NDC
- 71335-0707
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- morphine sulfate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120511
- Source listing expiry
- 20261231
Source-listed ingredients
- MORPHINE SULFATE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-1) · 71335-0707-1
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-2) · 71335-0707-2
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-3) · 71335-0707-3
- 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-4) · 71335-0707-4
- 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-5) · 71335-0707-5
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-6) · 71335-0707-6
- 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-7) · 71335-0707-7
- 8 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-8) · 71335-0707-8
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →