NDC 42689-007
Morphine Sulfate 50 mg capsule, extended release
On the label: Nortec Development Associates, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glatt Air Techniques, Inc. | Ramsey, NJ, United States | Makes it | No problems foundApr 13, 2023 · 8 inspections |
| SpecGx LLC | St. Louis, MO, United States | Makes the active ingredient | Problems found, fixed voluntarilyOct 22, 2025 · 8 inspections |
| ACTA Laboratories Inc | Foothill Ranch, CA, United States | Tests it | Problems found, fixed voluntarilySep 4, 2026 · 7 inspections |
| Alcami Carolinas Corporation | St. Louis, MO, United States | Tests it | Problems found, fixed voluntarilyOct 4, 2024 · 7 inspections |
| EMSL Analytical, Inc. DBA MPL Laboratories | Sparta, NJ, United States | Tests it | No problems foundJan 12, 2024 · 6 inspections |
| SGS North America Inc. | Fairfield, NJ, United States | Tests it | Problems found, fixed voluntarilyJun 9, 2026 · 8 inspections |
| Sharp Packaging Services, LLC | Allentown, PA, United States | Packages it | No problems foundNov 21, 2025 · 7 inspections |
Product details
- Generic drug
- Morphine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA203158
- On the market since
- Apr 7, 2009
- Package NDCs
42689-007-01- Official label
- DailyMed (National Library of Medicine), updated Aug 25, 2025
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