Product NDC: | 0409-1134 |
Proprietary Name: | Morphine Sulfate |
Non Proprietary Name: | MORPHINE SULFATE |
Active Ingredient(s): | 50 mg/mL & nbsp; MORPHINE SULFATE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-1134 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19960314 |
Package NDC: | 0409-1134-05 |
Package Description: | 1 VIAL in 1 CARTON (0409-1134-05) > 50 mL in 1 VIAL |
NDC Code | 0409-1134-05 |
Proprietary Name | Morphine Sulfate |
Package Description | 1 VIAL in 1 CARTON (0409-1134-05) > 50 mL in 1 VIAL |
Product NDC | 0409-1134 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | MORPHINE SULFATE |
Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
Route Name | INTRAVENOUS |
Start Marketing Date | 19960314 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Hospira, Inc. |
Substance Name | MORPHINE SULFATE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |