Product NDC: | 0574-0153 |
Proprietary Name: | morphine sulfate |
Non Proprietary Name: | Morphine Suldate |
Active Ingredient(s): | 100 mg/5mL & nbsp; Morphine Suldate |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0574-0153 |
Labeler Name: | Paddock Laboratories, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA201574 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120817 |
Package NDC: | 0574-0153-30 |
Package Description: | 1 BOTTLE in 1 CARTON (0574-0153-30) > 30 mL in 1 BOTTLE |
NDC Code | 0574-0153-30 |
Proprietary Name | morphine sulfate |
Package Description | 1 BOTTLE in 1 CARTON (0574-0153-30) > 30 mL in 1 BOTTLE |
Product NDC | 0574-0153 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Morphine Suldate |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20120817 |
Marketing Category Name | ANDA |
Labeler Name | Paddock Laboratories, LLC |
Substance Name | MORPHINE SULFATE |
Strength Number | 100 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |