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MORPHINE SULFATE
MORPHINE SULFATE - 0406-8330-62 - (MORPHINE SULFATE)
Drug Information of MORPHINE SULFATE
| Product NDC: | 0406-8330 |
| 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, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MORPHINE SULFATE
| Product NDC: | 0406-8330 |
| Labeler Name: | Mallinckrodt, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076412 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101021 |
Package Information of MORPHINE SULFATE
| Package NDC: | 0406-8330-62 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8330-62) |
NDC Information of MORPHINE SULFATE
| NDC Code | 0406-8330-62 |
| Proprietary Name | MORPHINE SULFATE |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8330-62) |
| Product NDC | 0406-8330 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MORPHINE SULFATE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20101021 |
| Marketing Category Name | ANDA |
| Labeler Name | Mallinckrodt, Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
