NDC codes

FDA NDC Directory
Product NDC (as listed)55154-4348Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55154-4348Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
55154-4348-555154434805551544348055 CUP in 1 BAG (55154-4348-5) / 10 mL in 1 CUPMarketed from Oct 31, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Cardinal Health 107, LLCNDC labeler code 55154
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 55154-4348_275a187a-5a49-4406-b325-e95f53441acdSPL ID 275a187a-5a49-4406-b325-e95f53441acd
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

N455154434805 followed by a unit qualifier and the quantity

Package 55154-4348-05. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 55154-4348

What is NDC 55154-4348?
55154-4348 is the product NDC for Sucralfate (sucralfate oral), Sucralfate 1 g/10mL suspension, listed with the FDA by Cardinal Health 107, LLC. It has 1 package NDC, 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?
Cardinal Health 107, LLC, NDC labeler code 55154. 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.

Other finished products listed under the same name: strengths, forms and labelers.

Other Sucralfate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
SucralfateSucralfate 1 g/10mLSuspensionOralSafecor Health, LLC48433-22648433-0226-40
SucralfateSucralfate 1 g/1TabletOralCardinal Health 107, LLC55154-028155154-0281-00
SucralfateSucralfate 1 g/1TabletOralSafecor Health LLC48433-09148433-0091-20
SucralfateSucralfate 1 g/10mLSuspensionOralTorrent Pharmaceuticals Limited13668-75413668-0754-42
SucralfateSucralfate 1 g/10mLSuspensionOralChartwell RX, LLC62135-10662135-0106-44
SucralfateSucralfate 1 g/10mLSuspensionOralChartwell Governmental & Specialty RX, LLC68999-10668999-0106-24
SucralfateSucralfate 1 g/1TabletOralCoupler LLC67046-146967046-1469-03
Sucralfatesucralfate oralSucralfate 1 g/10mLSuspensionOralPrecision Dose, Inc.68094-04168094-0041-6168094-0041-62
SucralfateSucralfate 1 g/10mLSuspensionOralCosette Pharmaceuticals, Inc.0713-079100713-0791-75
SucralfateSucralfate 1 g/1TabletOralPreferred Pharmaceuticals Inc68788-877968788-8779-0368788-8779-09

All 66 Sucralfate NDCs

Other NDCs under ANDA 209356

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 209356
ProductStrengthForm · routeLabelerProduct NDC
Sucralfatesucralfate oralSucralfate 1 g/10mLSuspensionOralAvKARE42291-781
Sucralfatesucralfate oralSucralfate 1 g/10mLSuspensionOralAvPAK50268-745
Sucralfatesucralfate oralSucralfate 1 g/10mLSuspensionOralAmneal Pharmaceuticals LLC65162-062
Sucralfatesucralfate oralSucralfate 1 g/10mLSuspensionOralPrecision Dose, Inc.68094-041

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