NDC codes

FDA NDC Directory
Product NDC (as listed)51079-753Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51079-0753Add 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
51079-753-2051079075320100 BLISTER PACK in 1 CARTON (51079-753-20) / 1 TABLET in 1 BLISTER PACK (51079-753-01)Marketed from Sep 24, 2013

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/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070848
Marketing start
Listing expires
Other FDA classes
Organometallic Compounds (Chemical structure)
Identifiers
Product ID 51079-753_3a87770c-fa4f-d061-e063-6294a90a6751SPL ID 3a87770c-fa4f-d061-e063-6294a90a6751SPL set ID 989ca8a8-3ad6-4ee4-aa9c-eed731828753RxCUI 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

N451079075320 followed by a unit qualifier and the quantity

Package 51079-0753-20. 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 070848

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

FDA NDC Directory listings under ANDA 070848
ProductStrengthForm · routeLabelerProduct NDC
SucralfateSucralfate 1 g/1TabletOralNorthwind Health Company, LLC51655-031
SucralfateSucralfate 1 g/1TabletOralCardinal Health 107, LLC55154-4379
SucralfateSucralfate 1 g/1TabletOralBryant Ranch Prepack63629-1307
SucralfateSucralfate 1 g/1TabletOralCardinal Health 107, LLC55154-0281
SucralfateSucralfate 1 g/1TabletOralDIRECT RX72189-234
SucralfateSucralfate 1 g/1TabletOralPreferred Pharmaceuticals Inc.68788-8946
SucralfateSucralfate 1 g/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-4517
SucralfateSucralfate 1 g/1TabletOralTeva Pharmaceuticals USA, Inc.0093-2210
SucralfateSucralfate 1 g/1TabletOralASCLEMED USA INC.87063-176
SucralfateSucralfate 1 g/1TabletOralAdvanced Rx of Tennessee, LLC80425-0091
SucralfateSucralfate 1 g/1TabletOralProficient Rx LP82804-063
SucralfateSucralfate 1 g/1TabletOralSafecor Health LLC48433-091
SucralfateSucralfate 1 g/1TabletOralNuCare Pharmaceuticals,Inc.68071-1749

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