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Sucralfate
Sucralfate - 49349-017-02 - (Sucralfate)
Drug Information of Sucralfate
| Product NDC: | 49349-017 |
| Proprietary Name: | Sucralfate |
| Non Proprietary Name: | Sucralfate |
| Active Ingredient(s): | 1 g/1 & nbsp; Sucralfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sucralfate
| Product NDC: | 49349-017 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018333 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100929 |
Package Information of Sucralfate
| Package NDC: | 49349-017-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-017-02) |
NDC Information of Sucralfate
| NDC Code | 49349-017-02 |
| Proprietary Name | Sucralfate |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-017-02) |
| Product NDC | 49349-017 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sucralfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100929 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | SUCRALFATE |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient] |
