Sucralfate
- Product NDC
- 60219-1656
- 11-digit product format
- 602191656
- Labeler code
- 60219
- Product ID
- 60219-1656_3595f982-2982-4ab0-838a-4cada5e1337b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA215576
- Marketing category
- ANDA
- Marketing start
- 2024-03-02
- 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
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUCRALFATE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | XX73205DH5 |
| Rxcui | 314234 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60219-1656-1 | Sucralfate | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 60219-1656-5 | Sucralfate | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60219-1656 | SUCRALFATE TABLET [AMNEAL PHARMACEUTICALS NY LLC] | 1 | Current NDC, 2 package rows | 20240303_b2e07ac7-4a8a-4b68-bb65-167d1aa86883.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 |
|---|
| 60219-1656-1 | 60219165601 | 100 TABLET in 1 BOTTLE (60219-1656-1) | 100 tablet | 2024-03-02 | No | No | Historical |
| 60219-1656-5 | 60219165605 | 500 TABLET in 1 BOTTLE (60219-1656-5) | 500 tablet | 2024-03-02 | No | No | Historical |