Sucralfate
- Product NDC
- 69339-148
- 11-digit product format
- 693390148
- Labeler code
- 69339
- Product ID
- 69339-148_3d0de6fb-6d76-4ad8-8cb6-cabd6d4513f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Dash Pharmaceuticals LLC
- Application
- NDA019183
- Marketing category
- NDA
- Marketing start
- 2021-01-27
- 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
- 2022-12-31
- 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 |
|---|
| 69339-148-17 | 69339014817 | 4 TRAY in 1 CASE (69339-148-17) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (69339-148-01) | 4 tray | 2021-01-27 | 0000-00-00 | No | No | Current |
| 69339-148-19 | 69339014819 | 10 TRAY in 1 CASE (69339-148-19) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (69339-148-01) | 10 tray | 2021-01-27 | 0000-00-00 | No | No | Current |