Product NDC: | 0406-8003 |
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: | 0406-8003 |
Labeler Name: | Mallinckrodt, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA202348 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111003 |
Package NDC: | 0406-8003-15 |
Package Description: | 6 CARTON in 1 CASE (0406-8003-15) > 1 BOTTLE, PLASTIC in 1 CARTON > 15 mL in 1 BOTTLE, PLASTIC |
NDC Code | 0406-8003-15 |
Proprietary Name | Morphine Sulfate |
Package Description | 6 CARTON in 1 CASE (0406-8003-15) > 1 BOTTLE, PLASTIC in 1 CARTON > 15 mL in 1 BOTTLE, PLASTIC |
Product NDC | 0406-8003 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | morphine sulfate |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20111003 |
Marketing Category Name | ANDA |
Labeler Name | Mallinckrodt, Inc. |
Substance Name | MORPHINE SULFATE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |