Sucralfate oral suspension
- Product NDC
- 68462-827
- 11-digit product format
- 684620827
- Labeler code
- 68462
- Product ID
- 68462-827_1e595c2a-edd0-43f7-a2db-69553b9557d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Application
- ANDA212141
- Marketing category
- ANDA
- Marketing start
- 2026-01-05
- Substance
- SUCRALFATE
- Active strength
- 1 g/10mL
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sucralfate oral suspension
- Listing expiration
- 2027-12-31
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 |
|---|
| 68462-827-61 | Sucralfate oral suspension | 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 |
|---|
| 68462-827-61 | 68462082761 | 420 mL in 1 BOTTLE (68462-827-61) | 420 ml | 2026-01-05 | No | No | Current |