Sucralfate
- Product NDC
- 13668-754
- 11-digit product format
- 136680754
- Labeler code
- 13668
- Product ID
- 13668-754_fd033c55-d1ae-4fbb-82ad-b092a20bb7e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA216726
- Marketing category
- ANDA
- Marketing start
- 2025-09-15
- 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 |
|---|
| 13668-754-42 | Sucralfate | 420 mL in 1 BOTTLE | SUSPENSION | 420 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 13668-754-42 | 13668075442 | 420 mL in 1 BOTTLE (13668-754-42) | 420 ml | 2025-09-15 | No | No | Current |