sucralfate
- Product NDC
- 72162-2479
- 11-digit product format
- 721622479
- Labeler code
- 72162
- Product ID
- 72162-2479_4e5200dd-dd65-48be-8dfd-e8411029de9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA216474
- Marketing category
- ANDA
- Marketing start
- 2024-07-10
- Substance
- SUCRALFATE
- Active strength
- 1 g/10mL
- 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/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | XX73205DH5 |
| Rxcui | 313123 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2479-2 | sucralfate | 420 mL in 1 BOTTLE | SUSPENSION | 420 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2479 | SUCRALFATE SUSPENSION [BRYANT RANCH PREPACK] | 102 | Current NDC, 1 package rows | 20250511_abc44549-ac41-4aef-9b15-2ba536e1555f.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 |
|---|
| 72162-2479-2 | 72162247902 | 420 mL in 1 BOTTLE (72162-2479-2) | 420 ml | 2025-05-01 | No | No | Current |