Product NDC: | 0527-1425 |
Proprietary Name: | Morphine Sulfate |
Non Proprietary Name: | Morphine Sulfate |
Active Ingredient(s): | 100 mg/5mL & nbsp; Morphine Sulfate |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0527-1425 |
Labeler Name: | Lannett Company, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA201517 |
Marketing Category: | NDA |
Start Marketing Date: | 20110623 |
Package NDC: | 0527-1425-35 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0527-1425-35) > 15 mL in 1 BOTTLE, PLASTIC |
NDC Code | 0527-1425-35 |
Proprietary Name | Morphine Sulfate |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0527-1425-35) > 15 mL in 1 BOTTLE, PLASTIC |
Product NDC | 0527-1425 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Morphine Sulfate |
Dosage Form Name | SOLUTION, CONCENTRATE |
Route Name | ORAL |
Start Marketing Date | 20110623 |
Marketing Category Name | NDA |
Labeler Name | Lannett Company, Inc. |
Substance Name | MORPHINE SULFATE |
Strength Number | 100 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |