Sucralfate
- Product NDC
- 60687-695
- 11-digit product format
- 606870695
- Labeler code
- 60687
- Product ID
- 60687-695_37dbc9fb-25b5-30a2-e063-6294a90a78b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA074415
- Marketing category
- ANDA
- Marketing start
- 2023-05-11
- Marketing end
- 2026-07-31
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sucralfate
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUCRALFATE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | XX73205DH5 |
| Rxcui | 314234 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-695-01 | Sucralfate | 100 in 1 CARTON | TABLET | 100 | | 3 |
| 60687-695-11 | Sucralfate | 1 in 1 BLISTER PACK | TABLET | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-695 | SUCRALFATE TABLET [AMERICAN HEALTH PACKAGING] | 2 | Current NDC, 2 package rows | 20241022_e7364686-3638-4061-ae4a-62b1df7af9d0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-695-01 | 60687069501 | 100 BLISTER PACK in 1 CARTON (60687-695-01) / 1 TABLET in 1 BLISTER PACK (60687-695-11) | 100 blister pack | 2023-05-11 | 2026-07-31 | No | No | Historical |
| 60687-695-11 | 60687069511 | 1 in 1 BLISTER PACK | | | | | | Historical |