Sucralfate
- Product NDC
- 42291-781
- 11-digit product format
- 422910781
- Labeler code
- 42291
- Product ID
- 42291-781_45107b4b-d201-c653-e063-6294a90a122d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate Oral
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA209356
- Marketing category
- ANDA
- Marketing start
- 2021-04-16
- 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 |
|---|
| 42291-781-42 | Sucralfate | 420 mL in 1 BOTTLE | SUSPENSION | 420 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42291-781 | SUCRALFATE (SUCRALFATE ORAL) SUSPENSION [AVKARE] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240111_c019bf24-8273-8d2f-e053-2a95a90aec98.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-781-42 | 42291078142 | 420 mL in 1 BOTTLE (42291-781-42) | 420 ml | 2021-04-16 | 0000-00-00 | No | No | Current |