Sucralfate
- Product NDC
- 72189-429
- 11-digit product format
- 721890429
- Labeler code
- 72189
- Product ID
- 72189-429_2c4d741e-e60b-2e62-e063-6294a90a65fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA074415
- Marketing category
- ANDA
- Marketing start
- 2023-03-02
- 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 |
|---|
| 72189-429-20 | Sucralfate | 20 in 1 BOTTLE | TABLET | 20 | | 2 |
| 72189-429-90 | Sucralfate | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-429 | SUCRALFATE TABLET [DIRECT_RX] | 2 | Current NDC, 2 package rows | 20250123_f5f0fecb-949c-3998-e053-2a95a90aac8c.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 |
|---|
| 72189-429-20 | 72189042920 | 20 TABLET in 1 BOTTLE (72189-429-20) | 20 tablet | 2023-03-02 | No | No | Current |
| 72189-429-90 | 72189042990 | 90 TABLET in 1 BOTTLE (72189-429-90) | 90 tablet | 2023-03-02 | No | No | Current |