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NDC 68788-8946-01 Sucralfate 1 g/1 Details
Sucralfate 1 g/1
Sucralfate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is SUCRALFATE.
MedlinePlus Drug Summary
Sucralfate is used to treat and prevent the return of duodenal ulcers (ulcers located in first part of the small intestine). Treatment with other medications, such as antibiotics, may also be necessary to treat and prevent the return of ulcers caused by a certain type of bacteria (H. pylori) Sucralfate is in a class of medications called protectants. It sticks to damaged ulcer tissue and protects against acid and enzymes so healing can occur.
Related Packages: 68788-8946-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Sucralfate
Product Information
| NDC | 68788-8946 |
|---|---|
| Product ID | 68788-8946_aebe7d47-2d63-4441-8856-3c13e82e0e99 |
| Associated GPIs | 49300010000305 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Sucralfate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Sucralfate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | g/1 |
| Substance Name | SUCRALFATE |
| Labeler Name | Preferred Pharmaceuticals Inc. |
| Pharmaceutical Class | Aluminum Complex [EPC], Organometallic Compounds [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA070848 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68788-8946-01 (68788894601)
| NDC Package Code | 68788-8946-1 |
|---|---|
| Billing NDC | 68788894601 |
| Package | 100 TABLET in 1 BOTTLE (68788-8946-1) |
| Marketing Start Date | 2015-10-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |