Sucralfate
- Product NDC
- 68094-171
- 11-digit product format
- 680940171
- Labeler code
- 68094
- Product ID
- 68094-171_01842db0-5cdf-4368-a708-9c158232361e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Precision Dose Inc.
- Application
- NDA019183
- Marketing category
- NDA
- Marketing start
- 2003-08-21
- Marketing end
- 2021-04-30
- Substance
- SUCRALFATE
- Active strength
- 1 g/10mL
- Pharmacologic classes
- Aluminum Complex [EPC],Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68094-171-61 | 68094017161 | 10 TRAY in 1 CASE (68094-171-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-171-59) | 10 tray | 2003-08-21 | 2021-04-30 | No | No | Current |
| 68094-171-62 | 68094017162 | 3 TRAY in 1 CASE (68094-171-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-171-59) | 3 tray | 2003-08-21 | 2021-04-30 | No | No | Current |