Sucralfate
- Product NDC
- 87063-176
- 11-digit product format
- 870630176
- Labeler code
- 87063
- Product ID
- 87063-176_52122b7a-f718-404c-e063-6394a90a6daf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ASCLEMED USA INC.
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 1996-11-11
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sucralfate
- Listing expiration
- 2027-12-31
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#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87063-176-01 | 87063017601 | 100 TABLET in 1 BOTTLE (87063-176-01) | 100 tablet | 2026-05-18 | No | No | Historical |
| 87063-176-05 | 87063017605 | 500 TABLET in 1 BOTTLE (87063-176-05) | 500 tablet | 2026-05-18 | No | No | Historical |
| 87063-176-12 | 87063017612 | 120 TABLET in 1 BOTTLE (87063-176-12) | 120 tablet | 2026-05-18 | No | No | Historical |
| 87063-176-30 | 87063017630 | 30 TABLET in 1 BOTTLE (87063-176-30) | 30 tablet | 2026-05-18 | No | No | Historical |
| 87063-176-60 | 87063017660 | 60 TABLET in 1 BOTTLE (87063-176-60) | 60 tablet | 2026-05-18 | No | No | Historical |
| 87063-176-90 | 87063017690 | 90 TABLET in 1 BOTTLE (87063-176-90) | 90 tablet | 2026-05-18 | No | No | Historical |