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Morphine Sulfate
Morphine Sulfate - 66689-033-16 - (Morphine Sulfate)
Drug Information of Morphine Sulfate
| Product NDC: | 66689-033 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | Morphine Sulfate |
| Active Ingredient(s): | 20 mg/5mL & nbsp; Morphine Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morphine Sulfate
| Product NDC: | 66689-033 |
| Labeler Name: | VistaPharm Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201947 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120301 |
Package Information of Morphine Sulfate
| Package NDC: | 66689-033-16 |
| Package Description: | 500 mL in 1 BOTTLE (66689-033-16) |
NDC Information of Morphine Sulfate
| NDC Code | 66689-033-16 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 500 mL in 1 BOTTLE (66689-033-16) |
| Product NDC | 66689-033 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine Sulfate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | ANDA |
| Labeler Name | VistaPharm Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 20 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
