What is NDC 71335-2114?

71335-2114 is the product NDC for Sucralfate, Sucralfate 1 g/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 9 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-2114 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2114Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2114Add 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
71335-2114-0	7133521140071335211400	28 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0)Marketed from Jun 20, 2022
71335-2114-1	7133521140171335211401	100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1)Marketed from Jun 20, 2022
71335-2114-2	7133521140271335211402	60 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2)Marketed from Jun 20, 2022
71335-2114-3	7133521140371335211403	30 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3)Marketed from Jun 20, 2022
71335-2114-4	7133521140471335211404	20 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4)Marketed from Jun 20, 2022
71335-2114-6	7133521140671335211406	150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6)Marketed from Jun 20, 2022
71335-2114-7	7133521140771335211407	90 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7)Marketed from Jun 20, 2022
71335-2114-8	7133521140871335211408	40 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8)Marketed from Jun 20, 2022
71335-2114-9	7133521140971335211409	120 TABLET in 1 BOTTLE, PLASTIC (71335-2114-9)Marketed from Jun 20, 2022

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: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074415
Marketing start: Feb 17, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Organometallic Compounds (Chemical structure)
Identifiers: Product ID 71335-2114_fc506a9a-8d99-f22b-e053-6394a90ad6d9SPL ID fc506a9a-8d99-f22b-e053-6394a90ad6d9SPL set ID 370f5ac6-2c64-42ef-ab5d-075a473012f1RxCUI 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

N471335211400 followed by a unit qualifier and the quantity

Package 71335-2114-00. 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 May 22, 2023.

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 71335-2114

What is NDC 71335-2114?: 71335-2114 is the product NDC for Sucralfate, Sucralfate 1 g/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 9 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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 074415

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

FDA NDC Directory listings under ANDA 074415
Product	Strength	Form · route	Labeler	Product NDC
Sucralfate	Sucralfate 1 g/1	TabletOral	A-S Medication Solutions	50090-6455
Sucralfate	Sucralfate 1 g/1	TabletOral	Chartwell RX, LLC	62135-436
Sucralfate	Sucralfate 1 g/1	TabletOral	Bryant Ranch Prepack	63629-9152
Sucralfate	Sucralfate 1 g/1	TabletOral	Bryant Ranch Prepack	63629-9153
Sucralfate	Sucralfate 1 g/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3478
Sucralfate	Sucralfate 1 g/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-541
Sucralfate	Sucralfate 1 g/1	TabletOral	Bryant Ranch Prepack	72162-2264
Sucralfate	Sucralfate 1 g/1	TabletOral	Direct_Rx	72189-429
Sucralfate	Sucralfate 1 g/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0188
Sucralfate	Sucralfate 1 g/1	TabletOral	Proficient Rx LP	82804-102