Sucralfate
- Product NDC
- 72162-2264
- 11-digit product format
- 721622264
- Labeler code
- 72162
- Product ID
- 72162-2264_9d3d9afa-c2ff-4182-90cf-861c34752ed8
- 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 |
|---|
| 72162-2264-1 | Sucralfate | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 100 |
| 72162-2264-5 | Sucralfate | 500 in 1 BOTTLE, PLASTIC | TABLET | 500 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2264 | SUCRALFATE TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20240224_28d7d257-8545-4b9f-8412-8ba144502400.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2264-1 | 72162226401 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-2264-1) | 100 tablet | 2024-02-23 | No | No | Historical |
| 72162-2264-5 | 72162226405 | 500 TABLET in 1 BOTTLE, PLASTIC (72162-2264-5) | 500 tablet | 2024-02-23 | No | No | Historical |