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Morphine Sulfate
Morphine Sulfate - 0409-2028-02 - (MORPHINE SULFATE)
Drug Information of Morphine Sulfate
| Product NDC: | 0409-2028 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | MORPHINE SULFATE |
| Active Ingredient(s): | .5 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
| Product NDC: | 0409-2028 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019917 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19921030 |
Package Information of Morphine Sulfate
| Package NDC: | 0409-2028-02 |
| Package Description: | 10 CARTON in 1 CONTAINER (0409-2028-02) > 1 VIAL, SINGLE-DOSE in 1 CARTON > 30 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Morphine Sulfate
| NDC Code | 0409-2028-02 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 10 CARTON in 1 CONTAINER (0409-2028-02) > 1 VIAL, SINGLE-DOSE in 1 CARTON > 30 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-2028 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MORPHINE SULFATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19921030 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
