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MORPHINE SULFATE
MORPHINE SULFATE - 42549-659-56 - (MORPHINE SULFATE)
Drug Information of MORPHINE SULFATE
| Product NDC: | 42549-659 |
| Proprietary Name: | MORPHINE SULFATE |
| Non Proprietary Name: | MORPHINE SULFATE |
| Active Ingredient(s): | 30 mg/1 & nbsp; MORPHINE SULFATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MORPHINE SULFATE
| Product NDC: | 42549-659 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022207 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080317 |
Package Information of MORPHINE SULFATE
| Package NDC: | 42549-659-56 |
| Package Description: | 56 TABLET in 1 BOTTLE (42549-659-56) |
NDC Information of MORPHINE SULFATE
| NDC Code | 42549-659-56 |
| Proprietary Name | MORPHINE SULFATE |
| Package Description | 56 TABLET in 1 BOTTLE (42549-659-56) |
| Product NDC | 42549-659 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MORPHINE SULFATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080317 |
| Marketing Category Name | NDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
