Home
>
National Drug Code (NDC)
>
Sucralfate
Sucralfate - 66689-790-50 - (Sucralfate)
Drug Information of Sucralfate
| Product NDC: | 66689-790 |
| Proprietary Name: | Sucralfate |
| Non Proprietary Name: | Sucralfate |
| Active Ingredient(s): | 1 g/10mL & nbsp; Sucralfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sucralfate
| Product NDC: | 66689-790 |
| Labeler Name: | VistaPharm, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019183 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120816 |
Package Information of Sucralfate
| Package NDC: | 66689-790-50 |
| Package Description: | 5 TRAY in 1 CASE (66689-790-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-790-01) |
NDC Information of Sucralfate
| NDC Code | 66689-790-50 |
| Proprietary Name | Sucralfate |
| Package Description | 5 TRAY in 1 CASE (66689-790-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-790-01) |
| Product NDC | 66689-790 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sucralfate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20120816 |
| Marketing Category Name | NDA |
| Labeler Name | VistaPharm, Inc. |
| Substance Name | SUCRALFATE |
| Strength Number | 1 |
| Strength Unit | g/10mL |
| Pharmaceutical Classes | Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient] |
