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Carafate
Carafate - 54868-3735-0 - (Sucralfate)
Drug Information of Carafate
| Product NDC: | 54868-3735 |
| Proprietary Name: | Carafate |
| 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 Carafate
| Product NDC: | 54868-3735 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019183 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960312 |
Package Information of Carafate
| Package NDC: | 54868-3735-0 |
| Package Description: | 414 mL in 1 BOTTLE (54868-3735-0) |
NDC Information of Carafate
| NDC Code | 54868-3735-0 |
| Proprietary Name | Carafate |
| Package Description | 414 mL in 1 BOTTLE (54868-3735-0) |
| Product NDC | 54868-3735 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sucralfate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19960312 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | SUCRALFATE |
| Strength Number | 1 |
| Strength Unit | g/10mL |
| Pharmaceutical Classes | Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient] |
