Sucralfate
- Product NDC
- 71610-244
- 11-digit product format
- 716100244
- Labeler code
- 71610
- Product ID
- 71610-244_0cc6d501-f008-4e5c-90fc-e47ca504c300
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 1996-11-11
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71610-244-60 | Sucralfate | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
| 71610-244-70 | Sucralfate | 120 in 1 BOTTLE | TABLET | 120 | | 1 |
| 71610-244-94 | Sucralfate | 360 in 1 BOTTLE | TABLET | 360 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71610-244 | SUCRALFATE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC, 3 package rows | 20190315_14074f98-42b5-48a6-88e1-e943ab495236.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 71610-244-60 | 71610024460 | 90 in 1 BOTTLE | Historical |
| 71610-244-70 | 71610024470 | 120 in 1 BOTTLE | Historical |
| 71610-244-94 | 71610024494 | 360 in 1 BOTTLE | Historical |