What is NDC 48433-226?

48433-226 is the product NDC for Sucralfate, Sucralfate 1 g/10mL suspension, listed with the FDA by Safecor Health, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Safecor Health, LLC, NDC labeler code 48433. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sucralfate NDC 48433-226 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48433-226Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48433-0226Add 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 NDC	11-digit (billing)	Package	Copy
48433-226-40	4843302264048433022640	40 CUP, UNIT-DOSE in 1 CASE (48433-226-40) / 10 mL in 1 CUP, UNIT-DOSE (48433-226-10)Marketed from Jul 16, 2026

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
Active ingredients: Sucralfate — 1 g/10mL
Dosage form: Suspension
Route: Oral
Labeler: Safecor Health, LLCNDC labeler code 48433
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217126
Marketing start: Jul 16, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Organometallic Compounds (Chemical structure)
Identifiers: Product ID 48433-226_56bc4a66-18f6-0c11-e063-6294a90a7e26SPL ID 56bc4a66-18f6-0c11-e063-6294a90a7e26SPL set ID 526f6ebc-557c-4c53-8118-1907baa0820aRxCUI 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

N448433022640 followed by a unit qualifier and the quantity

Package 48433-0226-40. 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 Jul 16, 2026.

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.

Full label on DailyMed (opens in a new tab)

About NDC 48433-226

What is NDC 48433-226?: 48433-226 is the product NDC for Sucralfate, Sucralfate 1 g/10mL suspension, listed with the FDA by Safecor Health, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sucralfate.
What is the active ingredient?: Sucralfate.
Who is the labeler?: Safecor Health, LLC, NDC labeler code 48433. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
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
Sucralfatesucralfate oral	Sucralfate 1 g/10mL	SuspensionOral	Precision Dose, Inc.	68094-041	68094-0041-6168094-0041-62
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

All 66 Sucralfate NDCs

Other NDCs under ANDA 217126

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

FDA NDC Directory listings under ANDA 217126
Product	Strength	Form · route	Labeler	Product NDC
Sucralfate	Sucralfate 1 g/10mL	SuspensionOral	Cosette Pharmaceuticals, Inc.	0713-0791