Sucralfate
- Product NDC
- 82182-106
- 11-digit product format
- 821820106
- Labeler code
- 82182
- Product ID
- 82182-106_e171ec84-fb54-4598-a9e8-e37413ef2c64
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Pacific Pharma, Inc.
- Application
- NDA019183
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2024-02-01
- Substance
- SUCRALFATE
- Active strength
- 1 g/10mL
- 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/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | XX73205DH5 |
| Rxcui | 313123 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82182-106-14 | Sucralfate | 420 mL in 1 BOTTLE | SUSPENSION | 420 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82182-106 | SUCRALFATE SUSPENSION [PACIFIC PHARMA, INC.] | 1 | Current NDC, 1 package rows | 20240202_7407c58e-766f-4e93-a1bb-c77892ae0174.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 |
|---|
| 82182-106-14 | 82182010614 | 420 mL in 1 BOTTLE (82182-106-14) | 420 ml | 2024-02-01 | No | No | Historical |