| Product NDC: | 11704-235 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | Morphine Sulfate |
| Active Ingredient(s): | 10 mg/.7mL & nbsp; Morphine Sulfate |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11704-235 |
| Labeler Name: | Meridian Medical Technologies, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019999 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900712 |
| Package NDC: | 11704-235-01 |
| Package Description: | 1 SYRINGE in 1 POUCH (11704-235-01) > .7 mL in 1 SYRINGE |
| NDC Code | 11704-235-01 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 1 SYRINGE in 1 POUCH (11704-235-01) > .7 mL in 1 SYRINGE |
| Product NDC | 11704-235 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine Sulfate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19900712 |
| Marketing Category Name | NDA |
| Labeler Name | Meridian Medical Technologies, Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 10 |
| Strength Unit | mg/.7mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |