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Morphine Sulfate
Morphine Sulfate - 0574-7114-12 - (MORPHINE SULFATE)
Drug Information of Morphine Sulfate
| Product NDC: | 0574-7114 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | MORPHINE SULFATE |
| Active Ingredient(s): | 20 mg/1 & nbsp; MORPHINE SULFATE |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morphine Sulfate
| Product NDC: | 0574-7114 |
| Labeler Name: | Paddock Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900901 |
Package Information of Morphine Sulfate
| Package NDC: | 0574-7114-12 |
| Package Description: | 12 PACKET in 1 BOX (0574-7114-12) > 1 SUPPOSITORY in 1 PACKET |
NDC Information of Morphine Sulfate
| NDC Code | 0574-7114-12 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 12 PACKET in 1 BOX (0574-7114-12) > 1 SUPPOSITORY in 1 PACKET |
| Product NDC | 0574-7114 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MORPHINE SULFATE |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19900901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Paddock Laboratories, LLC |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
