Sucralfate
- Product NDC
- 63629-9152
- 11-digit product format
- 636299152
- Labeler code
- 63629
- Product ID
- 63629-9152_68eb54fd-5a5e-4803-a43e-1c3134416377
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074415
- Marketing category
- ANDA
- Marketing start
- 2020-02-17
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sucralfate
- Listing expiration
- 2026-12-31
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 |
|---|
| 63629-9152-1 | Sucralfate | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 102 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-9152 | SUCRALFATE TABLET [BRYANT RANCH PREPACK] | 102 | Current NDC, Legacy NDC, 1 package rows | 20240113_7b05323d-4695-41d7-8236-1e7b4e8f2a1e.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 |
|---|
| 63629-9152-1 | 63629915201 | 100 TABLET in 1 BOTTLE, PLASTIC (63629-9152-1) | 100 tablet | 2022-01-26 | 0000-00-00 | No | No | Current |