Sucralfate
- Product NDC
- 17856-1011
- 11-digit product format
- 178561011
- Labeler code
- 17856
- Product ID
- 17856-1011_628a6d23-de71-403a-a829-51d3332a318f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- NDA019183
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-01-27
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-1011-1 | 17856101101 | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1011-1) > 10 mL in 1 CUP, UNIT-DOSE (17856-1011-2) | 2022-07-08 | 0000-00-00 | No | No | Current |