Sucralfate
- Product NDC
- 48433-091
- 11-digit product format
- 484330091
- Labeler code
- 48433
- Product ID
- 48433-091_4ee49539-03a8-151e-e063-6294a90ab13a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Safecor Health LLC
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 2026-03-13
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- 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
- Listing expiration
- 2027-12-31
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 |
|---|
| 48433-091-01 | Sucralfate | 1 in 1 BLISTER PACK | TABLET | 1 | | 3 |
| 48433-091-20 | Sucralfate | 100 in 1 CARTON | TABLET | 100 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48433-091-01 | 48433009101 | 1 in 1 BLISTER PACK | | | | | Historical |
| 48433-091-20 | 48433009120 | 100 BLISTER PACK in 1 CARTON (48433-091-20) / 1 TABLET in 1 BLISTER PACK (48433-091-01) | 100 blister pack | 2026-03-13 | No | No | Historical |