NDC codes

FDA NDC Directory
Product NDC (as listed)65862-083Labeler and product segments. Claims need a package NDC.
Product NDC at billing width65862-0083Add 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
65862-083-016586200830165862008301100 mL in 1 BOTTLE (65862-083-01)Marketed from Apr 25, 2013
65862-083-50658620083506586200835050 mL in 1 BOTTLE (65862-083-50)Marketed from Apr 25, 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)
Cefadroxil
Generic name (nonproprietary)
cefadroxil
Active ingredients
Cefadroxil — 250 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 065349
Marketing start
Listing expires
Other FDA classes
Cephalosporins (Chemical structure)
Identifiers
Product ID 65862-083_74923cbc-7511-447d-b6b2-b2d0e805a0f5SPL ID 74923cbc-7511-447d-b6b2-b2d0e805a0f5SPL set ID 776a8dbc-e68e-4732-acf4-0133dca0f54cRxCUI 105171, 309048UNII 280111G160
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

N465862008301 followed by a unit qualifier and the quantity

Package 65862-0083-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Cefadroxil is indicated for the treatment of patients with infection caused by susceptible strains of the designated organisms in the following diseases: Urinary tract infections caused by E. coli, P. mirabilis, and Klebsiella species. Skin and skin structure infections caused by staphylococci and/or streptococci. Pharyngitis and/or tonsillitis caused by Streptococcus pyogenes (Group A beta-hemolytic streptococci). Note: Only penicillin by the intramuscular route of administration has been shown to be effective in the prophylaxis of rheumatic fever. Cefadroxil is generally effective in the eradication of streptococci from the oropharynx. However, data establishing the e…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 65862-083

What is NDC 65862-083?
65862-083 is the product NDC for Cefadroxil, Cefadroxil 250 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?
Cefadroxil.
What is the active ingredient?
Cefadroxil.
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 Cefadroxil?
39 other product NDCs are listed under this name. See all Cefadroxil 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 Cefadroxil NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
CefadroxilCefadroxil 500 mg/1CapsuleOralAdvanced Rx of Tennessee, LLC80425-043280425-0432-0180425-0432-0280425-0432-03
CefadroxilCefadroxil 500 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-040080425-0400-0180425-0400-0280425-0400-03
CefadroxilCefadroxil 500 mg/1CapsuleOralDirect_Rx72189-50672189-0506-0672189-0506-20
CefadroxilCefadroxil 500 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-847968788-8479-0268788-8479-03
CefadroxilCefadroxil 500 mg/1CapsuleOralDirect_Rx72189-44572189-0445-0672189-0445-20
CefadroxilCefadroxil 500 mg/1CapsuleOralREMEDYREPACK INC.70518-358070518-3580-0070518-3580-01
CefadroxilCefadroxil 500 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-019880425-0198-0180425-0198-0280425-0198-03
CefadroxilCefadroxil 500 mg/1CapsuleOralPreferred Pharmaceuticals, Inc.68788-826168788-8261-0268788-8261-03
CefadroxilCefadroxil 500 mg/1CapsuleOralDIRECT RX72189-10372189-0103-0672189-0103-20
CefadroxilCefadroxil 500 mg/1CapsuleOralRedPharm Drug, Inc.67296-172767296-1727-0167296-1727-02

All 40 Cefadroxil NDCs

Other NDCs under ANDA 065349

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

FDA NDC Directory listings under ANDA 065349
ProductStrengthForm · routeLabelerProduct NDC
CefadroxilCefadroxil 250 mg/5mLPowder, For suspensionOralNorthStar Rx LLC16714-389
CefadroxilCefadroxil 500 mg/5mLPowder, For suspensionOralNorthStar Rx LLC16714-390
CefadroxilCefadroxil 250 mg/5mLPowder, For suspensionOralRising Pharma Holdings, Inc.57237-097
CefadroxilCefadroxil 500 mg/5mLPowder, For suspensionOralRising Pharma Holdings, Inc.57237-098
CefadroxilCefadroxil 500 mg/5mLPowder, For suspensionOralAurobindo Pharma Limited65862-084

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