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Morphine sulfate
Morphine sulfate - 0228-3503-11 - (Morphine sulfate)
Drug Information of Morphine sulfate
| Product NDC: | 0228-3503 |
| 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): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morphine sulfate
| Product NDC: | 0228-3503 |
| Labeler Name: | Actavis Elizabeth LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020616 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20111111 |
Package Information of Morphine sulfate
| Package NDC: | 0228-3503-11 |
| Package Description: | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-3503-11) |
NDC Information of Morphine sulfate
| NDC Code | 0228-3503-11 |
| Proprietary Name | Morphine sulfate |
| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-3503-11) |
| Product NDC | 0228-3503 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine sulfate |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20111111 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Actavis Elizabeth LLC |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
