Sucralfate
- Product NDC
- 55154-5778
- 11-digit product format
- 551545778
- Labeler code
- 55154
- Product ID
- 55154-5778_4b18a21f-5990-4cc1-b36b-953c3ad85e40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- NDA019183
- Marketing category
- NDA
- Marketing start
- 2009-11-19
- Marketing end
- 2023-06-30
- Substance
- SUCRALFATE
- Active strength
- 1 g/10mL
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-5778-5 | 55154577805 | 5 CUP, UNIT-DOSE in 1 BAG (55154-5778-5) > 10 mL in 1 CUP, UNIT-DOSE | 2009-11-19 | 2023-06-30 | No | No | Current |