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 NDC11-digit (billing)PackageCopy
71335-2114-07133521140028 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0)Marketed from Jun 20, 2022
71335-2114-171335211401100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1)Marketed from Jun 20, 2022
71335-2114-27133521140260 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2)Marketed from Jun 20, 2022
71335-2114-37133521140330 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3)Marketed from Jun 20, 2022
71335-2114-47133521140420 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4)Marketed from Jun 20, 2022
71335-2114-671335211406150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6)Marketed from Jun 20, 2022
71335-2114-77133521140790 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7)Marketed from Jun 20, 2022
71335-2114-87133521140840 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8)Marketed from Jun 20, 2022
71335-2114-971335211409120 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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074415
Marketing start
Listing expires
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

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

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
ProductStrengthForm · routeLabelerProduct NDC
SucralfateSucralfate 1 g/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-541
SucralfateSucralfate 1 g/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0188
SucralfateSucralfate 1 g/1TabletOralDirect_Rx72189-429
SucralfateSucralfate 1 g/1TabletOralA-S Medication Solutions50090-6455
SucralfateSucralfate 1 g/1TabletOralBryant Ranch Prepack72162-2264
SucralfateSucralfate 1 g/1TabletOralBryant Ranch Prepack63629-9152
SucralfateSucralfate 1 g/1TabletOralBryant Ranch Prepack63629-9153
SucralfateSucralfate 1 g/1TabletOralNuCare Pharmaceuticals,Inc.68071-3478
SucralfateSucralfate 1 g/1TabletOralGolden State Medical Supply, Inc.51407-881
SucralfateSucralfate 1 g/1TabletOralChartwell RX, LLC62135-436
SucralfateSucralfate 1 g/1TabletOralProficient Rx LP82804-102

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