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Sucralfate
Sucralfate - 68094-171-62 - (Sucralfate)
Drug Information of Sucralfate
| Product NDC: | 68094-171 |
| 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: | 68094-171 |
| Labeler Name: | Precision Dose Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019183 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030821 |
Package Information of Sucralfate
| Package NDC: | 68094-171-62 |
| Package Description: | 3 TRAY in 1 CASE (68094-171-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-171-59) |
NDC Information of Sucralfate
| NDC Code | 68094-171-62 |
| Proprietary Name | Sucralfate |
| Package Description | 3 TRAY in 1 CASE (68094-171-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-171-59) |
| Product NDC | 68094-171 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sucralfate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20030821 |
| Marketing Category Name | NDA |
| Labeler Name | Precision Dose Inc. |
| Substance Name | SUCRALFATE |
| Strength Number | 1 |
| Strength Unit | g/10mL |
| Pharmaceutical Classes | Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient] |
