Sucralfate
- Product NDC
- 17856-0062
- 11-digit product format
- 178560062
- Labeler code
- 17856
- Product ID
- 17856-0062_a623642a-03f5-45e8-b151-374995d45401
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate Oral
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA209356
- Marketing category
- ANDA
- Marketing start
- 2019-12-02
- Marketing end
- 0000-00-00
- Substance
- SUCRALFATE
- Active strength
- 1 g/10mL
- Pharmacologic classes
- Aluminum Complex [EPC],Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0062-1 | Sucralfate | 72 in 1 BOX, UNIT-DOSE | SUSPENSION | 72 | | 2 |
| 17856-0062-1 | Sucralfate | 10 mL in 1 CUP, UNIT-DOSE | SUSPENSION | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0062 | SUCRALFATE (SUCRALFATE ORAL) SUSPENSION [ATLANTIC BIOLOGICALS CORP.] | 2 | Legacy NDC, 2 package rows | 20210112_573f74bc-6a49-4412-9eee-427536079851.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-0062-1 | 17856006201 | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0062-1) > 10 mL in 1 CUP, UNIT-DOSE | 2021-01-11 | 0000-00-00 | No | No | Current |