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Morphine Sulfate Injection
Morphine Sulfate Injection - 0409-1762-30 - (MORPHINE SULFATE)
Drug Information of Morphine Sulfate Injection
| Product NDC: | 0409-1762 |
| Proprietary Name: | Morphine Sulfate Injection |
| Non Proprietary Name: | MORPHINE SULFATE |
| Active Ingredient(s): | 2 mg/mL & nbsp; MORPHINE SULFATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morphine Sulfate Injection
| Product NDC: | 0409-1762 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19380101 |
Package Information of Morphine Sulfate Injection
| Package NDC: | 0409-1762-30 |
| Package Description: | 10 CARTRIDGE in 1 CARTON (0409-1762-30) > 1 mL in 1 CARTRIDGE |
NDC Information of Morphine Sulfate Injection
| NDC Code | 0409-1762-30 |
| Proprietary Name | Morphine Sulfate Injection |
| Package Description | 10 CARTRIDGE in 1 CARTON (0409-1762-30) > 1 mL in 1 CARTRIDGE |
| Product NDC | 0409-1762 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MORPHINE SULFATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19380101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Hospira, Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
