NDC 60687-738 – Sucralfate
Sucralfate 1 g/10mL · Suspension · Oral
Product NDC60687-738
Product details
- Brand name
- Sucralfate
- Generic name
- Sucralfate
- Labeler
- American Health Packaging
- Dosage form
- Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA211884
- Marketed since
- August 1, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aluminum Complex
Active ingredients
- Sucralfate 1 g/10mL
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 60687-738-08 | 3 TRAY in 1 CASE (60687-738-08) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42) | Aug 1, 2023 |
| 60687-738-23 | 4 TRAY in 1 CASE (60687-738-23) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42) | Aug 1, 2023 |
| 60687-738-56 | 10 TRAY in 1 CASE (60687-738-56) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42) | Aug 1, 2023 |
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