NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4970Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4970Add 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
68071-4970-6680714970066807149700660 mL in 1 BOTTLE (68071-4970-6)Marketed from Jul 18, 2019

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Cefdinir
Generic name (nonproprietary)
cefdinir
Active ingredients
Cefdinir — 125 mg/5mL
Dosage form
Powder, For suspension
Route
Oral
Labeler
NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065473
Marketing start
Listing expires
Other FDA classes
Cephalosporins (Chemical structure)
Identifiers
Product ID 68071-4970_1b2e8147-7c01-7d0a-e063-6394a90aeea1SPL ID 1b2e8147-7c01-7d0a-e063-6394a90aeea1SPL set ID 8dfbad95-4dd8-01fd-e053-2a95a90a1de1RxCUI 309054UNII CI0FAO63WCUPC 0368071497069
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

N468071497006 followed by a unit qualifier and the quantity

Package 68071-4970-06. 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 To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefdinir and other antibacterial drugs, cefdinir should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Cefdinir for oral suspension is indicated for the treatment of patients with mild to moderate infections caused by susceptible strains of the designated …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-4970

What is NDC 68071-4970?
68071-4970 is the product NDC for Cefdinir, Cefdinir 125 mg/5mL powder, for suspension, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cefdinir.
What is the active ingredient?
Cefdinir.
Who is the labeler?
NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cefdinir?
80 other product NDCs are listed under this name. See all Cefdinir 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 Cefdinir NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
CefdinirCefdinir 250 mg/5mLPowder, For suspensionOralPreferred Pharmaceuticals Inc.68788-410668788-4106-01
CefdinirCefdinir 300 mg/1CapsuleOralMajor Pharmaceuticals0904-756300904-7563-04
CefdinirCefdinir 300 mg/1CapsuleOralREMEDYREPACK INC.70518-416970518-4169-0070518-4169-0170518-4169-02+1 more
CefdinirCefdinir 300 mg/1CapsuleOralNorthwind Health Company, LLC82868-05982868-0059-20
CefdinirCefdinir 300 mg/1CapsuleOralAvKARE42291-04342291-0043-60
CefdinirCefdinir monohydrate 250 mg/5mLPowder, For suspensionOralPreferred Pharmaceuticals Inc.68788-865568788-8655-01
CefdinirCefdinir 300 mg/1CapsuleOralAmerican Health Packaging60687-69960687-0699-21
CefdinirCefdinir 300 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-840468788-8404-02
CefdinirCefdinir 300 mg/1CapsuleOralDirect_Rx72189-42372189-0423-1472189-0423-20
CefdinirCefdinir 300 mg/1CapsuleOralPreferred Pharmaceuticals, Inc.68788-832368788-8323-02

All 81 Cefdinir NDCs

Other NDCs under ANDA 065473

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

FDA NDC Directory listings under ANDA 065473
ProductStrengthForm · routeLabelerProduct NDC
CefdinirCefdinir 250 mg/5mLPowder, For suspensionOralA-S Medication Solutions50090-2735
CefdinirCefdinir 125 mg/5mLPowder, For suspensionOralA-S Medication Solutions50090-6417
CefdinirCefdinir 125 mg/5mLPowder, For suspensionOralProficient Rx LP63187-835
CefdinirCefdinir 125 mg/5mLPowder, For suspensionOralAurobindo Pharma Limited65862-218
CefdinirCefdinir 250 mg/5mLPowder, For suspensionOralAurobindo Pharma Limited65862-219
CefdinirCefdinir 250 mg/5mLPowder, For suspensionOralNuCare Pharmaceuticals,Inc.68071-5106
CefdinirCefdinir 125 mg/5mLPowder, For suspensionOralNuCare Pharmaceuticals, Inc.68071-5318
CefdinirCefdinir 250 mg/5mLPowder, For suspensionOralPreferred Pharmaceuticals Inc.68788-7844
CefdinirCefdinir 250 mg/5mLPowder, For suspensionOralProficient Rx LP71205-405
CefdinirCefdinir 125 mg/5mLPowder, For suspensionOralDIRECT RX72189-185
CefdinirCefdinir 250 mg/5mLPowder, For suspensionOralDIRECT RX72189-186

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