Sucralfate
- Product NDC
- 70518-3959
- 11-digit product format
- 705183959
- Labeler code
- 70518
- Product ID
- 70518-3959_3bb32136-21fc-131e-e063-6394a90ab24f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA215705
- Marketing category
- ANDA
- Marketing start
- 2023-12-13
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sucralfate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUCRALFATE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | XX73205DH5 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3959-0 | Sucralfate | 30 in 1 BLISTER PACK | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3959 | SUCRALFATE TABLET [REMEDYREPACK INC.] | 3 | Current NDC, 1 package rows | 20240405_c0ee24dd-de9c-4d24-b8d8-c45b02752c1c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-3959-0 | 70518395900 | 30 TABLET in 1 BLISTER PACK (70518-3959-0) | 30 tablet | 2023-12-13 | No | No | Current |