Sucralfate
- Product NDC
- 70934-446
- 11-digit product format
- 709340446
- Labeler code
- 70934
- Product ID
- 70934-446_a79981d4-c1aa-e58a-e053-2a95a90a1247
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- NDA018333
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-09-24
- Marketing end
- 0000-00-00
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC],Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-446-30 | 70934044630 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-446-30) | 30 tablet | 2019-09-24 | 0000-00-00 | No | No | Current |