Sucralfate
- Product NDC
- 0121-0747
- 11-digit product format
- 001210747
- Labeler code
- 0121
- Product ID
- 0121-0747_d554fc2f-929a-72a1-e053-2a95a90a6f20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- NDA019183
- Marketing category
- NDA
- Marketing start
- 2009-11-19
- 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 |
|---|
| 0121-0747-00 | 00121074700 | 10 TRAY in 1 CASE (0121-0747-00) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-0747-10) | 10 tray | 2009-11-19 | 0000-00-00 | No | No | Current |
| 0121-0747-30 | 00121074730 | 3 TRAY in 1 CASE (0121-0747-30) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-0747-10) | 3 tray | 2009-11-19 | 0000-00-00 | No | No | Current |
| 0121-0747-40 | 00121074740 | 4 TRAY in 1 CASE (0121-0747-40) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-0747-10) | 4 tray | 2020-04-28 | 0000-00-00 | No | No | Current |
| 0121-0747-50 | 00121074750 | 5 TRAY in 1 CASE (0121-0747-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-0747-10) | 5 tray | 2020-04-29 | 0000-00-00 | No | No | Current |