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MORPHINE SULFATE
MORPHINE SULFATE - 35356-521-60 - (MORPHINE SULFATE)
Drug Information of MORPHINE SULFATE
| Product NDC: | 35356-521 |
| Proprietary Name: | MORPHINE SULFATE |
| Non Proprietary Name: | MORPHINE SULFATE |
| Active Ingredient(s): | 100 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: | 35356-521 |
| Labeler Name: | Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076438 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110728 |
Package Information of MORPHINE SULFATE
| Package NDC: | 35356-521-60 |
| Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (35356-521-60) |
NDC Information of MORPHINE SULFATE
| NDC Code | 35356-521-60 |
| Proprietary Name | MORPHINE SULFATE |
| Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (35356-521-60) |
| Product NDC | 35356-521 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MORPHINE SULFATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110728 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
