Home
>
National Drug Code (NDC)
>
Morphine Sulfate
Morphine Sulfate - 68084-160-01 - (Morphine Sulfate)
Drug Information of Morphine Sulfate
| Product NDC: | 68084-160 |
| 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, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morphine Sulfate
| Product NDC: | 68084-160 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074769 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130621 |
Package Information of Morphine Sulfate
| Package NDC: | 68084-160-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-160-01) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-160-11) |
NDC Information of Morphine Sulfate
| NDC Code | 68084-160-01 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-160-01) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-160-11) |
| Product NDC | 68084-160 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine Sulfate |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130621 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
