Sucralfate
- Product NDC
- 0904-7269
- 11-digit product format
- 009047269
- Labeler code
- 0904
- Product ID
- 0904-7269_ec83e1ee-e504-0759-e053-2995a90a22a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- MAJOR
- Application
- ANDA211884
- Marketing category
- ANDA
- Marketing start
- 2022-03-15
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7269 | SUCRALFATE SUSPENSION [MAJOR PHARMACEUTICALS] | 5 | Legacy NDC | 20240126_ec83e1ee-e503-0759-e053-2995a90a22a5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7269-18 | 00904726918 | 4 TRAY in 1 CASE (0904-7269-18) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0904-7269-66) | 4 tray | 2022-11-02 | 0000-00-00 | No | No | Current |