What is NDC 51407-334?

51407-334 is the product NDC for Cefuroxime axetil, Cefuroxime axetil 500 mg/1 tablet, film coated, listed with the FDA by Golden State Medical Supply, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Golden State Medical Supply, Inc., NDC labeler code 51407. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Cefuroxime axetil?

40 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cefuroxime axetil NDC 51407-334 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51407-334Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51407-0334Add 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
51407-334-20	5140703342051407033420	20 TABLET, FILM COATED in 1 BOTTLE (51407-334-20)Marketed from Jan 29, 2021
51407-334-60	5140703346051407033460	60 TABLET, FILM COATED in 1 BOTTLE (51407-334-60)Marketed from Jan 29, 2021

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): Cefuroxime axetil
Generic name (nonproprietary): cefuroxime axetil
Active ingredients: Cefuroxime axetil — 500 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Golden State Medical Supply, Inc.NDC labeler code 51407
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 065496
Marketing start: Jun 7, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Cephalosporins (Chemical structure)
Identifiers: Product ID 51407-334_502429f5-1f55-2030-e063-6394a90aef14SPL ID 502429f5-1f55-2030-e063-6394a90aef14SPL set ID bb7955fe-5111-1662-e053-2a95a90a85a1RxCUI 309097, 309098UNII Z49QDT0J8ZUPC 0351407334602, 0351407333209
Pharmacologic class: Cephalosporin Antibacterial

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

N451407033420 followed by a unit qualifier and the quantity

Package 51407-0334-20. 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

Current FDA label (SPL), effective Apr 23, 2026.

Indications (excerpt from the label)

Cefuroxime axetil tablet is a cephalosporin antibacterial drug indicated for the treatment of the following infections due to susceptible bacteria: (1) Pharyngitis/tonsillitis (adults and pediatric patients) ( 1.1 ) Acute bacterial otitis media (pediatric patients) ( 1.2 ) Acute bacterial maxillary sinusitis (adults and pediatric patients) ( 1.3 ) Acute bacterial exacerbations of chronic bronchitis (adults and pediatric patients 13 years and older) ( 1.4 ) Uncomplicated skin and skin-structure infections (adults and pediatric patients 13 years and older) ( 1.5 ) Uncomplicated urinary tract infections (adults and pediatric patients 13 years and older) ( 1.6 ) Uncomplicated gonorrhea (adults a…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51407-334

What is NDC 51407-334?: 51407-334 is the product NDC for Cefuroxime axetil, Cefuroxime axetil 500 mg/1 tablet, film coated, listed with the FDA by Golden State Medical Supply, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cefuroxime axetil.
What is the active ingredient?: Cefuroxime axetil.
Who is the labeler?: Golden State Medical Supply, Inc., NDC labeler code 51407. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cefuroxime axetil?: 40 other product NDCs are listed under this name. See all Cefuroxime axetil 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 Cefuroxime axetil NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0571	80425-0571-0180425-0571-02
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7542	00904-7542-10
Cefuroxime Axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8905	68788-8905-02
Cefuroxime Axetil	Cefuroxime axetil 250 mg/1	TabletOral	Coupler LLC	67046-1307	67046-1307-03
Cefuroxime Axetil	Cefuroxime axetil 500 mg/1	TabletOral	Coupler LLC	67046-1081	67046-1081-03
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-283	60687-0283-94
Cefuroxime Axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-3215	70518-3215-04
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-272	60687-0272-94
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-656	43063-0656-1443063-0656-20
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-657	43063-0657-2043063-0657-60

All 41 Cefuroxime axetil NDCs

Other NDCs under ANDA 065496

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

FDA NDC Directory listings under ANDA 065496
Product	Strength	Form · route	Labeler	Product NDC
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals, Inc.	68071-3975
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-333
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-272
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-283
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-035
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0571
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-4947
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-1637
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-216
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7542
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-215
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-991
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2159
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2157
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2158
Cefuroxime axetil	Cefuroxime axetil 500 mg/1	Tablet, Film coatedOral	Redpharm Drug	67296-2168
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-656
Cefuroxime axetil	Cefuroxime axetil 250 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-657