Sucralfate
- Product NDC
- 62135-436
- 11-digit product format
- 621350436
- Labeler code
- 62135
- Product ID
- 62135-436_3ba3bac9-79bb-7f76-e063-6294a90a4d32
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- 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 |
|---|
| 62135-436-01 | Sucralfate | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 62135-436-90 | Sucralfate | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-436 | SUCRALFATE TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20230317_30c0965a-02a0-46b5-aa09-3f5fb5047b22.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 |
|---|
| 62135-436-01 | 62135043601 | 100 TABLET in 1 BOTTLE (62135-436-01) | 100 tablet | 2023-03-13 | | No | No | Historical |
| 62135-436-90 | 62135043690 | 90 TABLET in 1 BOTTLE (62135-436-90) | 90 tablet | 2022-11-04 | 0000-00-00 | No | No | Current |