Sucralfate
- Product NDC
- 55154-8133
- 11-digit product format
- 551548133
- Labeler code
- 55154
- Product ID
- 55154-8133_3e7e9db7-4ccd-4085-8414-7c7bf92dcfc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 2016-03-14
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-8133-0 | 55154813300 | 1 BLISTER PACK in 1 BAG (55154-8133-0) > 10 TABLET in 1 BLISTER PACK | 1 blister pack | 2016-03-14 | 0000-00-00 | No | No | Current |