Sucralfate
- Product NDC
- 81033-149
- 11-digit product format
- 810330149
- Labeler code
- 81033
- Product ID
- 81033-149_36d940f2-207c-68c5-e063-6294a90a6b4a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Kesin Pharma Corporation
- Application
- ANDA216474
- Marketing category
- ANDA
- Marketing start
- 2024-07-01
- 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 |
|---|
| 81033-149-10 | Sucralfate | 10 mL in 1 CUP, UNIT-DOSE | SUSPENSION | 10 | | 1 |
| 81033-149-44 | Sucralfate | 40 in 1 CARTON | SUSPENSION | 40 | | 1 |
| 81033-149-52 | Sucralfate | 100 in 1 CASE | SUSPENSION | 100 | | 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 |
|---|
| 81033-149-10 | 81033014910 | 10 mL in 1 CUP, UNIT-DOSE | 10 ml | | | | Historical |
| 81033-149-44 | 81033014944 | 40 CUP, UNIT-DOSE in 1 CARTON (81033-149-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10) | | 2024-07-01 | No | No | Current |
| 81033-149-52 | 81033014952 | 100 CUP, UNIT-DOSE in 1 CASE (81033-149-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10) | | 2024-07-01 | No | No | Current |