Sucralfate
- Product NDC
- 68094-043
- 11-digit product format
- 680940043
- Labeler code
- 68094
- Product ID
- 68094-043_0bd354cc-3e14-47e0-a350-d19f3383bbb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Precision Dose, Inc.
- Application
- NDA019183
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-03-19
- Marketing end
- 0000-00-00
- Substance
- SUCRALFATE
- Active strength
- 1 g/10mL
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68094-043-61 | 68094004361 | 10 TRAY in 1 CASE (68094-043-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-043-59) | 10 tray | 2020-03-19 | 0000-00-00 | No | No | Current |
| 68094-043-62 | 68094004362 | 3 TRAY in 1 CASE (68094-043-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-043-59) | 3 tray | 2020-03-19 | 0000-00-00 | No | No | Current |