SUCRALFATE
- Product NDC
- 72189-234
- 11-digit product format
- 721890234
- Labeler code
- 72189
- Product ID
- 72189-234_2c285743-2fa6-4132-e063-6294a90adaff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SUCRALFATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 2021-06-18
- 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 |
|---|
| 72189-234-20 | SUCRALFATE | 20 in 1 BOTTLE | TABLET | 20 | | 4 |
| 72189-234-90 | SUCRALFATE | 90 in 1 BOTTLE | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-234 | SUCRALFATE TABLET [DIRECT RX] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250121_c50b5044-31ed-672a-e053-2995a90a49fc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-234-20 | 72189023420 | 20 TABLET in 1 BOTTLE (72189-234-20) | 20 tablet | 2021-06-18 | 0000-00-00 | No | No | Current |
| 72189-234-90 | 72189023490 | 90 TABLET in 1 BOTTLE (72189-234-90) | 90 tablet | 2021-06-18 | 0000-00-00 | No | No | Current |