What is NDC 64380-149?

64380-149 is the product NDC for sucralfate, Sucralfate 1 g/10mL suspension, listed with the FDA by Strides Pharma Science Limited. It has 6 package NDCs, shown above in 10- and 11-digit form.

Strides Pharma Science Limited, NDC labeler code 64380. 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 64380-149 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)64380-149Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64380-0149Add 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
64380-149-01	6438001490164380014901	420 mL in 1 BOTTLE, PLASTIC (64380-149-01)Marketed from Jul 10, 2024
64380-149-03	6438001490364380014903	5 CUP, UNIT-DOSE in 1 TRAY (64380-149-03) / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)Marketed from Jul 10, 2024
64380-149-04	6438001490464380014904	3 TRAY in 1 CARTON (64380-149-04) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)Marketed from Jul 10, 2024
64380-149-05	6438001490564380014905	4 TRAY in 1 CARTON (64380-149-05) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)Marketed from Jul 10, 2024
64380-149-06	6438001490664380014906	5 TRAY in 1 CARTON (64380-149-06) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)Marketed from Jul 10, 2024
64380-149-07	6438001490764380014907	10 TRAY in 1 CARTON (64380-149-07) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)Marketed from Jul 10, 2024

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: Strides Pharma Science LimitedNDC labeler code 64380
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216474
Marketing start: Jul 10, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Organometallic Compounds (Chemical structure)
Identifiers: Product ID 64380-149_a60083fe-4fc9-444d-a210-184ca92a4716SPL ID a60083fe-4fc9-444d-a210-184ca92a4716SPL set ID 8e25bff2-769e-4bd4-a6de-895c58b840d2RxCUI 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

N464380014901 followed by a unit qualifier and the quantity

Package 64380-0149-01. 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

Current FDA label (SPL), effective Mar 10, 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 64380-149

What is NDC 64380-149?: 64380-149 is the product NDC for sucralfate, Sucralfate 1 g/10mL suspension, listed with the FDA by Strides Pharma Science Limited. It has 6 package NDCs, 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?: Strides Pharma Science Limited, NDC labeler code 64380. 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 216474

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

FDA NDC Directory listings under ANDA 216474
Product	Strength	Form · route	Labeler	Product NDC
sucralfate	Sucralfate 1 g/10mL	SuspensionOral	Bryant Ranch Prepack	72162-2479
Sucralfate	Sucralfate 1 g/10mL	SuspensionOral	Kesin Pharma Corporation	81033-149