Prescription drug · ANDA
Sucralfate (Sucralfate oral) NDC 68094-041
Sucralfate 1 g/10mL · Suspension · Oral · Precision Dose, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68094-041-61 | 6809400416168094004161 | 10 TRAY in 1 CASE (68094-041-61) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)Marketed from Jan 30, 2025 | |
| 68094-041-62 | 6809400416268094004162 | 3 TRAY in 1 CASE (68094-041-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)Marketed from Jan 30, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Sucralfate
- Generic name (nonproprietary)
- sucralfate oral
- Active ingredients
- Sucralfate — 1 g/10mL
- Dosage form
- Suspension
- Route
- Oral
- Labeler
- Precision Dose, Inc.NDC labeler code 68094
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 209356
- Marketing start
- Listing expires
- Other FDA classes
- Organometallic Compounds (Chemical structure)
- Identifiers
- Product ID 68094-041_f2fb0919-1f13-4ca2-bf04-254c1e44b86cSPL ID f2fb0919-1f13-4ca2-bf04-254c1e44b86cSPL set ID 0dc592e9-541c-4fac-8ab5-829d43521c01RxCUI 313123UNII XX73205DH5
- Pharmacologic class
- Aluminum Complex
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N468094004161followed by a unit qualifier and the quantityPackage 68094-0041-61. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE Sucralfate Oral Suspension is indicated in the short-term (up to 8 weeks) treatment of active duodenal ulcer.
Excerpt only. Read the full label for complete information.
About NDC 68094-041
- What is NDC 68094-041?
- 68094-041 is the product NDC for Sucralfate (sucralfate oral), Sucralfate 1 g/10mL suspension, listed with the FDA by Precision Dose, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Sucralfate (Sucralfate oral).
- What is the active ingredient?
- Sucralfate.
- Who is the labeler?
- Precision Dose, Inc., NDC labeler code 68094. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Sucralfate?
- 65 other product NDCs are listed under this name. See all Sucralfate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Sucralfate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Sucralfate | Sucralfate 1 g/10mL | SuspensionOral | Safecor Health, LLC | 48433-226 | 48433-0226-40 |
| Sucralfate | Sucralfate 1 g/1 | TabletOral | Cardinal Health 107, LLC | 55154-0281 | 55154-0281-00 |
| Sucralfate | Sucralfate 1 g/1 | TabletOral | Safecor Health LLC | 48433-091 | 48433-0091-20 |
| Sucralfate | Sucralfate 1 g/10mL | SuspensionOral | Torrent Pharmaceuticals Limited | 13668-754 | 13668-0754-42 |
| Sucralfate | Sucralfate 1 g/10mL | SuspensionOral | Chartwell RX, LLC | 62135-106 | 62135-0106-44 |
| Sucralfate | Sucralfate 1 g/10mL | SuspensionOral | Chartwell Governmental & Specialty RX, LLC | 68999-106 | 68999-0106-24 |
| Sucralfate | Sucralfate 1 g/1 | TabletOral | Coupler LLC | 67046-1469 | 67046-1469-03 |
| Sucralfate | Sucralfate 1 g/10mL | SuspensionOral | Cosette Pharmaceuticals, Inc. | 0713-0791 | 00713-0791-75 |
| Sucralfate | Sucralfate 1 g/1 | TabletOral | Preferred Pharmaceuticals Inc | 68788-8779 | 68788-8779-0368788-8779-09 |
| Sucralfate | Sucralfate 1 g/10mL | SuspensionOral | Richmond Pharmaceuticals, Inc. | 54738-005 | 54738-0005-42 |
Other NDCs under ANDA 209356
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Sucralfatesucralfate oral | Sucralfate 1 g/10mL | SuspensionOral | AvKARE | 42291-781 |
| Sucralfatesucralfate oral | Sucralfate 1 g/10mL | SuspensionOral | AvPAK | 50268-745 |
| Sucralfatesucralfate oral | Sucralfate 1 g/10mL | SuspensionOral | Cardinal Health 107, LLC | 55154-4348 |
| Sucralfatesucralfate oral | Sucralfate 1 g/10mL | SuspensionOral | Amneal Pharmaceuticals LLC | 65162-062 |