Home
>
National Drug Code (NDC)
>
morphine sulfate
morphine sulfate - 60951-659-70 - (morphine sulfate)
Drug Information of morphine sulfate
| Product NDC: | 60951-659 |
| Proprietary Name: | morphine sulfate |
| Non Proprietary Name: | morphine sulfate |
| Active Ingredient(s): | 200 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: | 60951-659 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075295 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981031 |
Package Information of morphine sulfate
| Package NDC: | 60951-659-70 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60951-659-70) |
NDC Information of morphine sulfate
| NDC Code | 60951-659-70 |
| Proprietary Name | morphine sulfate |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60951-659-70) |
| Product NDC | 60951-659 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | morphine sulfate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19981031 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
