NDC codes

FDA NDC Directory
Product NDC (as listed)14335-730Labeler and product segments. Claims need a package NDC.
Product NDC at billing width14335-0730Add 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
14335-730-1014335073010143350730101 VIAL, SINGLE-USE in 1 CARTON (14335-730-10) / 20 mL in 1 VIAL, SINGLE-USEMarketed from Nov 20, 2025

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)
Voriconazole
Generic name (nonproprietary)
voriconazole
Active ingredients
Voriconazole — 10 mg/mL
Dosage form
Injection, Solution
Route
Intravenous
Labeler
Hainan Poly Pharm. Co., Ltd.NDC labeler code 14335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 220043
Marketing start
Listing expires
Other FDA classes
Azoles (Chemical structure)Cytochrome P450 2C19 Inhibitors (Mechanism)Cytochrome P450 2C9 Inhibitors (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)
Identifiers
Product ID 14335-730_4ce54074-b0ac-3c98-e063-6394a90a9131SPL ID 4ce54074-b0ac-3c98-e063-6394a90a9131SPL set ID 393a81ba-7d51-450e-8d20-23287767c002RxCUI 2727399UNII JFU09I87TRUPC 0314335730014
Pharmacologic class
Azole Antifungal

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N414335073010 followed by a unit qualifier and the quantity

Package 14335-0730-10. 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)

Voriconazole injection is an azole antifungal indicated for the treatment of adults and pediatric patients 2 years of age and older with: Invasive aspergillosis ( 1.1 ) Candidemia in non-neutropenics and other deep tissue Candida infections ( 1.2 ) Esophageal candidiasis ( 1.3 ) Serious fungal infections caused by Scedosporium apiospermum and Fusarium species including Fusarium solani , in patients intolerant of, or refractory to, other therapy ( 1.4 ) 1.1 Invasive Aspergillosis Voriconazole injection is indicated in adults and pediatric patients (2 years of age and older) for the treatment of invasive aspergillosis (IA). In clinical trials, the majority of isolates recovered were Aspergillu…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 14335-730

What is NDC 14335-730?
14335-730 is the product NDC for Voriconazole, Voriconazole 10 mg/mL injection, solution, listed with the FDA by Hainan Poly Pharm. Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Voriconazole.
What is the active ingredient?
Voriconazole.
Who is the labeler?
Hainan Poly Pharm. Co., Ltd., NDC labeler code 14335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Voriconazole?
51 other product NDCs are listed under this name. See all Voriconazole 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 Voriconazole NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
VoriconazoleVoriconazole 50 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-96860687-0968-21
VoriconazoleVoriconazole 200 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-97960687-0979-21
Voriconazolevoriconazole injectionVoriconazole 10 mg/mLInjectionIntravenousPAI Holdings, LLC dba PAI Pharma0121-109100121-1091-55
VoriconazoleVoriconazole 50 mg/1Tablet, Film coatedOralSafecor Health LLC48433-14648433-0146-03
VoriconazoleVoriconazole 200 mg/1Tablet, Film coatedOralSafecor Health LLC48433-14748433-0147-03
VoriconazoleVoriconazole 40 mg/mLPowder, For suspensionOralCamber Pharmaceuticals, Inc.31722-26631722-0266-31
voriconazoleVoriconazole 200 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-119872162-1198-03
voriconazoleVoriconazole 40 mg/mLPowder, For suspensionOralZhejiang Poly Pharm Co., Ltd.72673-11172673-0111-30
VoriconazoleVoriconazole 10 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousCamber Pharmaceuticals, Inc.31722-22431722-0224-31
voriconazoleVoriconazole 40 mg/mLPowder, For suspensionOralSlate Run Pharmaceuticals, LLC70436-23070436-0230-39

All 52 Voriconazole NDCs

Other NDCs under ANDA 220043

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

FDA NDC Directory listings under ANDA 220043
ProductStrengthForm · routeLabelerProduct NDC
Voriconazolevoriconazole injectionVoriconazole 10 mg/mLInjectionIntravenousPAI Holdings, LLC dba PAI Pharma0121-1091

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