Home
>
National Drug Code (NDC)
>
Morphine Sulfate
Morphine Sulfate - 48433-200-01 - (morphine sulfate)
Drug Information of Morphine Sulfate
| Product NDC: | 48433-200 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | morphine sulfate |
| Active Ingredient(s): | 20 mg/mL & nbsp; morphine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morphine Sulfate
| Product NDC: | 48433-200 |
| Labeler Name: | Safecor Health, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202348 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130117 |
Package Information of Morphine Sulfate
| Package NDC: | 48433-200-01 |
| Package Description: | 1 mL in 1 SYRINGE (48433-200-01) |
NDC Information of Morphine Sulfate
| NDC Code | 48433-200-01 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 1 mL in 1 SYRINGE (48433-200-01) |
| Product NDC | 48433-200 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | morphine sulfate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20130117 |
| Marketing Category Name | ANDA |
| Labeler Name | Safecor Health, LLC |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
