What is NDC 65862-752?

65862-752 is the product NDC for Cefixime, Cefixime 200 mg/5mL powder, for suspension, listed with the FDA by Aurobindo Pharma Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 65862. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Cefixime?

10 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cefixime NDC 65862-752 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)65862-752Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65862-0752Add 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
65862-752-50	65862075250	50 mL in 1 BOTTLE (65862-752-50)Marketed from Apr 14, 2015
65862-752-75	65862075275	75 mL in 1 BOTTLE (65862-752-75)Marketed from Apr 14, 2015

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): Cefixime
Generic name (nonproprietary): cefixime
Active ingredients: Cefixime — 200 mg/5mL
Dosage form: Powder, For suspension
Route: Oral
Labeler: Aurobindo Pharma LimitedNDC labeler code 65862
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204835
Marketing start: Apr 14, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Cephalosporins (Chemical structure)
Identifiers: Product ID 65862-752_141b12c3-31de-4ca7-ac89-d864975846abSPL ID 141b12c3-31de-4ca7-ac89-d864975846abSPL set ID 068e6edd-a5fe-40d8-8dcf-ac82b78dced4RxCUI 309058, 419849UNII 97I1C92E55
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

N465862075250 followed by a unit qualifier and the quantity

Package 65862-0752-50. 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 Feb 14, 2024.

Indications (excerpt from the label)

Cefixime for oral suspension is a cephalosporin antibacterial drug indicated in the treatment of adults and pediatric patients six months and older with the following infections: Uncomplicated Urinary Tract Infections (1.1) Otitis Media (1.2) Pharyngitis and Tonsillitis (1.3) Acute Exacerbations of Chronic Bronchitis (1.4) Uncomplicated Gonorrhea (cervical/urethral) (1.5) To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefixime for oral suspension and other antibacterial drugs, cefixime for oral suspension should be used only to treat infections that are proven or strongly suspected to be caused by bacteria. (1.6) 1.1 Uncomplicated Urinary Tract Infecti…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 65862-752

What is NDC 65862-752?: 65862-752 is the product NDC for Cefixime, Cefixime 200 mg/5mL powder, for suspension, listed with the FDA by Aurobindo Pharma Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cefixime.
What is the active ingredient?: Cefixime.
Who is the labeler?: Aurobindo Pharma Limited, NDC labeler code 65862. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cefixime?: 10 other product NDCs are listed under this name. See all Cefixime 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 Cefixime NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cefixime	Cefixime 400 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4759	70518-4759-00
Cefixime	Cefixime 400 mg/1	CapsuleOral	Aurobindo Pharma Limited	59651-647	59651-0647-1059651-0647-50
Cefixime	Cefixime 400 mg/1	TabletOral	Rising Pharma Holdings, Inc.	64980-430	64980-0430-01
Cefixime	Cefixime 400 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3221	70518-3221-0270518-3221-04
Cefixime	Cefixime 400 mg/1	CapsuleOral	Lupin Pharmaceuticals, Inc.	68180-423	68180-0423-0868180-0423-11
Cefixime	Cefixime 400 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-2749	70518-2749-0270518-2749-05
Cefixime	Cefixime 400 mg/1	CapsuleOral	Ascend Laboratories, LLC	67877-584	67877-0584-0167877-0584-0567877-0584-33+1 more
Cefixime	Cefixime 200 mg/5mL	Powder, For suspensionOral	Lupin Pharmaceuticals, Inc.	68180-407	68180-0407-0368180-0407-04
Cefixime	Cefixime 100 mg/5mL	Powder, For suspensionOral	Lupin Pharmaceuticals, Inc.	68180-405	68180-0405-01
Cefixime	Cefixime 100 mg/5mL	Powder, For suspensionOral	Aurobindo Pharma Limited	65862-751	65862-0751-0165862-0751-50

Other NDCs under ANDA 204835

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

FDA NDC Directory listings under ANDA 204835
Product	Strength	Form · route	Labeler	Product NDC
Cefixime	Cefixime 100 mg/5mL	Powder, For suspensionOral	Aurobindo Pharma Limited	65862-751