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Morphine Sulfate
Morphine Sulfate - 0409-3815-12 - (Morphine Sulfate)
Drug Information of Morphine Sulfate
| Product NDC: | 0409-3815 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | Morphine Sulfate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Morphine Sulfate |
| Administration Route(s): | EPIDURAL; INTRATHECAL; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morphine Sulfate
| Product NDC: | 0409-3815 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073510 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120305 |
Package Information of Morphine Sulfate
| Package NDC: | 0409-3815-12 |
| Package Description: | 5 VIAL, GLASS in 1 CARTON (0409-3815-12) > 10 mL in 1 VIAL, GLASS |
NDC Information of Morphine Sulfate
| NDC Code | 0409-3815-12 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 5 VIAL, GLASS in 1 CARTON (0409-3815-12) > 10 mL in 1 VIAL, GLASS |
| Product NDC | 0409-3815 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine Sulfate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | EPIDURAL; INTRATHECAL; INTRAVENOUS |
| Start Marketing Date | 20120305 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
