What is NDC 67046-1469?

67046-1469 is the product NDC for Sucralfate, Sucralfate 1 g/1 tablet, listed with the FDA by Coupler LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Coupler LLC, NDC labeler code 67046. 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 67046-1469 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67046-1469Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67046-1469Add 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
67046-1469-3	6704614690367046146903	30 TABLET in 1 BLISTER PACK (67046-1469-3)Marketed from Feb 4, 2025

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
Active ingredients: Sucralfate — 1 g/1
Dosage form: Tablet
Route: Oral
Labeler: Coupler LLCNDC labeler code 67046
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215705
Marketing start: Feb 4, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Organometallic Compounds (Chemical structure)
Identifiers: Product ID 67046-1469_2d5893c4-5f80-adea-e063-6294a90ae3e9SPL ID 2d5893c4-5f80-adea-e063-6294a90ae3e9SPL set ID 2d586736-73ae-9af0-e063-6294a90ad875RxCUI 314234UNII 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

N467046146903 followed by a unit qualifier and the quantity

Package 67046-1469-03. 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 Feb 4, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Sucralfate tablets are indicated in: Short-term treatment (up to 8 weeks) of active duodenal ulcer. While healing with sucralfate may occur during the first week or two, treatment should be continued for 4 to 8 weeks unless healing has been demonstrated by x-ray or endoscopic examination. Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67046-1469

What is NDC 67046-1469?: 67046-1469 is the product NDC for Sucralfate, Sucralfate 1 g/1 tablet, listed with the FDA by Coupler 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?: Coupler LLC, NDC labeler code 67046. 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/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
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 215705

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

FDA NDC Directory listings under ANDA 215705
Product	Strength	Form · route	Labeler	Product NDC
Sucralfate	Sucralfate 1 g/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8653
Sucralfate	Sucralfate 1 g/1	TabletOral	Redpharm Drug	67296-2147
Sucralfate	Sucralfate 1 g/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3812
Sucralfate	Sucralfate 1 g/1	TabletOral	Preferred Pharmaceuticals Inc	68788-8779
Sucralfate	Sucralfate 1 g/1	TabletOral	Zydus Lifesciences Limited	70771-1833
Sucralfate	Sucralfate 1 g/1	TabletOral	Bryant Ranch Prepack	71335-2461
Sucralfate	Sucralfate 1 g/1	TabletOral	Viona Pharmaceuticals Inc	72578-081