Sucralfate
- Product NDC
- 50268-732
- 11-digit product format
- 502680732
- Labeler code
- 50268
- Product ID
- 50268-732_d5e0c734-93ac-61e3-e053-2a95a90ad520
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate Oral
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA209356
- Marketing category
- ANDA
- Marketing start
- 2020-08-17
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-732-12 | 50268073212 | 20 CUP in 1 BOX (50268-732-12) > 10 mL in 1 CUP (50268-732-11) | 20 cup | 2020-08-17 | 0000-00-00 | No | No | Current |