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SUCRALFATE
SUCRALFATE - 16590-523-60 - (SUCRALFATE)
Drug Information of SUCRALFATE
| Product NDC: | 16590-523 |
| 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: | 16590-523 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074415 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090701 |
Package Information of SUCRALFATE
| Package NDC: | 16590-523-60 |
| Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (16590-523-60) |
NDC Information of SUCRALFATE
| NDC Code | 16590-523-60 |
| Proprietary Name | SUCRALFATE |
| Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (16590-523-60) |
| Product NDC | 16590-523 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SUCRALFATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | SUCRALFATE |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient] |
