What is NDC 67296-2147?

67296-2147 is the product NDC for Sucralfate, Sucralfate 1 g/1 tablet, listed with the FDA by Redpharm Drug. It has 1 package NDC, shown above in 10- and 11-digit form.

Redpharm Drug, NDC labeler code 67296. 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 67296-2147 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67296-2147Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67296-2147Add 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
67296-2147-4	6729621470467296214704	40 TABLET in 1 BOTTLE (67296-2147-4)Marketed from May 20, 2023

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: Redpharm DrugNDC labeler code 67296
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215705
Marketing start: May 20, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Organometallic Compounds (Chemical structure)
Identifiers: Product ID 67296-2147_4637f5d7-c529-1d00-e063-6394a90a754fSPL ID 4637f5d7-c529-1d00-e063-6394a90a754fSPL set ID 3251e156-4c52-63b3-e063-6294a90a9a95RxCUI 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

N467296214704 followed by a unit qualifier and the quantity

Package 67296-2147-04. 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 Dec 18, 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 67296-2147

What is NDC 67296-2147?: 67296-2147 is the product NDC for Sucralfate, Sucralfate 1 g/1 tablet, listed with the FDA by Redpharm Drug. 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?: Redpharm Drug, NDC labeler code 67296. 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
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

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	Coupler LLC	67046-1469
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