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Morphine Sulfate
Morphine Sulfate - 0548-1911-25 - (Morphine Sulfate)
Drug Information of Morphine Sulfate
| Product NDC: | 0548-1911 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | Morphine Sulfate |
| Active Ingredient(s): | 30 mg/30mL & nbsp; Morphine Sulfate |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morphine Sulfate
| Product NDC: | 0548-1911 |
| Labeler Name: | Amphastar Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19870327 |
Package Information of Morphine Sulfate
| Package NDC: | 0548-1911-25 |
| Package Description: | 10 SYRINGE in 1 CARTON (0548-1911-25) > 30 mL in 1 SYRINGE (0548-1911-00) |
NDC Information of Morphine Sulfate
| NDC Code | 0548-1911-25 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 10 SYRINGE in 1 CARTON (0548-1911-25) > 30 mL in 1 SYRINGE (0548-1911-00) |
| Product NDC | 0548-1911 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine Sulfate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19870327 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Amphastar Pharmaceuticals, Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 30 |
| Strength Unit | mg/30mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
