Sucralfate NDC 60219-1656

NDC codes

FDA NDC Directory

Product NDC (as listed)60219-1656Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60219-1656Add 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
60219-1656-1	60219165601	100 TABLET in 1 BOTTLE (60219-1656-1)Marketed from Mar 2, 2024
60219-1656-5	60219165605	500 TABLET in 1 BOTTLE (60219-1656-5)Marketed from Mar 2, 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
Active ingredients: Sucralfate — 1 g/1
Dosage form: Tablet
Route: Oral
Labeler: Amneal Pharmaceuticals NY LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215576
Marketing start: Mar 2, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Organometallic Compounds (Chemical structure)
Identifiers: Product ID 60219-1656_3595f982-2982-4ab0-838a-4cada5e1337bSPL ID 3595f982-2982-4ab0-838a-4cada5e1337bSPL set ID b2e07ac7-4a8a-4b68-bb65-167d1aa86883RxCUI 314234UNII XX73205DH5UPC 0360219165618
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

N460219165601 followed by a unit qualifier and the quantity

Package 60219-1656-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 215576

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

FDA NDC Directory listings under ANDA 215576
Product	Strength	Form · route	Labeler	Product NDC
Sucralfate	Sucralfate 1 g/1	TabletOral	AvKARE	42291-936
Sucralfate	Sucralfate 1 g/1	TabletOral	Amneal Pharmaceuticals NY LLC	69238-1656