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) |
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 NDC: | 48433-200-55 |
Package Description: | .5 mL in 1 SYRINGE (48433-200-55) |
NDC Code | 48433-200-55 |
Proprietary Name | Morphine Sulfate |
Package Description | .5 mL in 1 SYRINGE (48433-200-55) |
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] |