What is NDC 68999-106?

68999-106 is the product NDC for Sucralfate, Sucralfate 1 g/10mL suspension, listed with the FDA by Chartwell Governmental & Specialty RX, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Chartwell Governmental & Specialty RX, LLC, NDC labeler code 68999. 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?

67 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 68999-106 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68999-106Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68999-0106Add 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
68999-106-24	68999010624	2 TRAY in 1 BOX (68999-106-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-106-10)Marketed from Sep 8, 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: Chartwell Governmental & Specialty RX, LLCNDC labeler code 68999
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211780
Marketing start: Apr 14, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Organometallic Compounds (Chemical structure)
Identifiers: Product ID 68999-106_5ba17da1-6576-02fd-e063-6294a90a21a1SPL ID 5ba17da1-6576-02fd-e063-6294a90a21a1
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

N468999010624 followed by a unit qualifier and the quantity

Package 68999-0106-24. 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 68999-106

What is NDC 68999-106?: 68999-106 is the product NDC for Sucralfate, Sucralfate 1 g/10mL suspension, listed with the FDA by Chartwell Governmental & Specialty RX, 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?: Chartwell Governmental & Specialty RX, LLC, NDC labeler code 68999. 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?: 67 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/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 68 Sucralfate NDCs

Other NDCs under ANDA 211780

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

FDA NDC Directory listings under ANDA 211780
Product	Strength	Form · route	Labeler	Product NDC
Sucralfate	Sucralfate 1 g/10mL	SuspensionOral	Chartwell RX, LLC	62135-106