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Morphine Sulfate
Morphine Sulfate - 49884-835-01 - (Morphine Sulfate)
Drug Information of Morphine Sulfate
| Product NDC: | 49884-835 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | Morphine Sulfate |
| Active Ingredient(s): | 50 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: | 49884-835 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020616 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121109 |
Package Information of Morphine Sulfate
| Package NDC: | 49884-835-01 |
| Package Description: | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-835-01) |
NDC Information of Morphine Sulfate
| NDC Code | 49884-835-01 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-835-01) |
| Product NDC | 49884-835 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine Sulfate |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20121109 |
| Marketing Category Name | NDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
