SUCRALFATE
- Product NDC
- 76519-1025
- 11-digit product format
- 765191025
- Labeler code
- 76519
- Product ID
- 76519-1025_740cc2a8-8103-2df2-e053-2991aa0ae507
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SUCRALFATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 2016-01-28
- 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
- 2019-12-31
- 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 |
|---|
| 76519-1025-0 | SUCRALFATE | 98 in 1 VIAL, PLASTIC | TABLET | 98 | | 1 |
| 76519-1025-1 | SUCRALFATE | 100 in 1 VIAL, PLASTIC | TABLET | 100 | | 1 |
| 76519-1025-6 | SUCRALFATE | 60 in 1 VIAL, PLASTIC | TABLET | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76519-1025 | SUCRALFATE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 3 package rows | 20180823_73fbec5b-a63c-5909-e053-2991aa0a2142.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76519-1025-0 | 76519102500 | 98 in 1 VIAL, PLASTIC | Historical |
| 76519-1025-1 | 76519102501 | 100 in 1 VIAL, PLASTIC | Historical |
| 76519-1025-6 | 76519102506 | 60 in 1 VIAL, PLASTIC | Historical |