NDC codes

FDA NDC Directory
Product NDC (as listed)16714-390Labeler and product segments. Claims need a package NDC.
Product NDC at billing width16714-0390Add 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
16714-390-01167140390011671403900175 mL in 1 BOTTLE (16714-390-01)Marketed from Apr 25, 2013
16714-390-021671403900216714039002100 mL in 1 BOTTLE (16714-390-02)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 — 500 mg/5mL
Dosage form
Powder, For suspension
Route
Oral
Labeler
NorthStar Rx LLCNDC labeler code 16714
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 16714-390_323b9a4d-c8fc-4fdb-bba4-834468a0a770SPL ID 323b9a4d-c8fc-4fdb-bba4-834468a0a770SPL set ID 30bb3686-87b4-4676-9ff5-e20deb8bff9dRxCUI 105171, 309048UNII 280111G160UPC 0316714390024, 0316714389011
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

N416714039001 followed by a unit qualifier and the quantity

Package 16714-0390-01. 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 16714-390

What is NDC 16714-390?
16714-390 is the product NDC for Cefadroxil, Cefadroxil 500 mg/5mL powder, for suspension, listed with the FDA by NorthStar Rx LLC. 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?
NorthStar Rx LLC, NDC labeler code 16714. 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 250 mg/5mLPowder, For suspensionOralRising Pharma Holdings, Inc.57237-097
CefadroxilCefadroxil 500 mg/5mLPowder, For suspensionOralRising Pharma Holdings, Inc.57237-098
CefadroxilCefadroxil 250 mg/5mLPowder, For suspensionOralAurobindo Pharma Limited65862-083
CefadroxilCefadroxil 500 mg/5mLPowder, For suspensionOralAurobindo Pharma Limited65862-084

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