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MORPHINE SULFATE
MORPHINE SULFATE - 0574-0127-30 - (MORPHINE SULFATE)
Drug Information of MORPHINE SULFATE
| Product NDC: | 0574-0127 |
| 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: | 0574-0127 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091008 |
Package Information of MORPHINE SULFATE
| Package NDC: | 0574-0127-30 |
| Package Description: | 1 BOTTLE in 1 CARTON (0574-0127-30) > 30 mL in 1 BOTTLE |
NDC Information of MORPHINE SULFATE
| NDC Code | 0574-0127-30 |
| Proprietary Name | MORPHINE SULFATE |
| Package Description | 1 BOTTLE in 1 CARTON (0574-0127-30) > 30 mL in 1 BOTTLE |
| Product NDC | 0574-0127 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MORPHINE SULFATE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091008 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
