Product NDC: | 52533-045 |
Proprietary Name: | Morphine Sulfate |
Non Proprietary Name: | Morphine Sulfate |
Active Ingredient(s): | 40 mg/mL & nbsp; Morphine Sulfate |
Administration Route(s): | INTRATHECAL |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52533-045 |
Labeler Name: | Cantrell Drug Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120824 |
Package NDC: | 52533-045-39 |
Package Description: | 20 mL in 1 SYRINGE, PLASTIC (52533-045-39) |
NDC Code | 52533-045-39 |
Proprietary Name | Morphine Sulfate |
Package Description | 20 mL in 1 SYRINGE, PLASTIC (52533-045-39) |
Product NDC | 52533-045 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Morphine Sulfate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRATHECAL |
Start Marketing Date | 20120824 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cantrell Drug Company |
Substance Name | MORPHINE SULFATE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |