NDC codes

FDA NDC Directory
Product NDC (as listed)25021-190Labeler and product segments. Claims need a package NDC.
Product NDC at billing width25021-0190Add 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
25021-190-10250210190101 VIAL in 1 CARTON (25021-190-10) / 5 mL in 1 VIALMarketed from Jun 15, 2021
25021-190-112502101901110 VIAL in 1 CARTON (25021-190-11) / 5 mL in 1 VIALMarketed from Sep 15, 2022
25021-190-122502101901220 VIAL in 1 CARTON (25021-190-12) / 5 mL in 1 VIALMarketed from Nov 1, 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)
Micafungin
Generic name (nonproprietary)
micafungin sodium
Active ingredients
Micafungin sodium — 50 mg/5mL
Dosage form
Injection, Powder, Lyophilized, For solution
Route
Intravenous
Labeler
Sagent PharmaceuticalsNDC labeler code 25021
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213363
Marketing start
Listing expires
Other FDA classes
Lipopeptides (Chemical structure)
Identifiers
Product ID 25021-190_edf05767-b6ad-4236-ac59-6c63ec6869f0SPL ID edf05767-b6ad-4236-ac59-6c63ec6869f0SPL set ID 33e579c1-b315-44cb-a690-e2dd2cdf44eeRxCUI 861379, 861383UNII IS1UP79R56
Pharmacologic class
Echinocandin 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

N425021019010 followed by a unit qualifier and the quantity

Package 25021-0190-10. 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)

Micafungin for injection is indicated for: Treatment of Candidemia, Acute Disseminated Candidiasis, Candida Peritonitis and Abscesses in adult and pediatric patients 4 months of age and older [see Clinical Studies ( 14.1 ) and Use in Specific Populations ( 8.4 )]. Treatment of Candidemia, Acute Disseminated Candidiasis, Candida Peritonitis and Abscesses without meningoencephalitis and/or ocular dissemination in pediatric patients younger than 4 months of age [see Use in Specific Populations ( 8.4 )] . Treatment of Esophageal Candidiasis in adult and pediatric patients 4 months of age and older [see Clinical Studies ( 14.2 )]. Prophylaxis of Candida Infections in adult and pediatric patients …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 25021-190

What is NDC 25021-190?
25021-190 is the product NDC for Micafungin (micafungin sodium), Micafungin sodium 50 mg/5mL injection, powder, lyophilized, for solution, listed with the FDA by Sagent Pharmaceuticals. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Micafungin (Micafungin Sodium).
What is the active ingredient?
Micafungin sodium.
Who is the labeler?
Sagent Pharmaceuticals, NDC labeler code 25021. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Micafungin?
20 other product NDCs are listed under this name. See all Micafungin 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 Micafungin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
MicafunginMicafungin sodium 50 mg/1Injection, Powder, For solutionIntravenousHisun Pharmaceuticals USA, Inc.42658-02242658-0022-0142658-0022-02
MicafunginMicafungin sodium 100 mg/1Injection, Powder, For solutionIntravenousHisun Pharmaceuticals USA, Inc.42658-02342658-0023-0142658-0023-02
MicafunginMicafungin 10 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousGlenmark Pharmaceuticals Inc., USA68462-77168462-0771-0168462-0771-10
MicafunginMicafungin 20 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousGlenmark Pharmaceuticals Inc., USA68462-77268462-0772-0168462-0772-10
MicafunginMicafungin sodium 10 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousBiocon Pharma Inc.70377-07570377-0075-91
MicafunginMicafungin sodium 20 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousBiocon Pharma Inc.70377-07670377-0076-91
MicafunginMicafungin 10 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousQilu Pharmaceutical Co., Ltd67184-058967184-0589-0167184-0589-02
MicafunginMicafungin 20 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousQilu Pharmaceutical Co., Ltd67184-059067184-0590-0167184-0590-02
MicafunginMicafungin sodium 10 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousZydus Pharmaceuticals USA Inc.70710-172470710-1724-0170710-1724-06
MicafunginMicafungin sodium 20 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousZydus Pharmaceuticals USA Inc.70710-172570710-1725-0170710-1725-06

All 21 Micafungin NDCs

Other NDCs under ANDA 213363

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

FDA NDC Directory listings under ANDA 213363
ProductStrengthForm · routeLabelerProduct NDC
Micafunginmicafungin sodiumMicafungin sodium 100 mg/5mLInjection, Powder, Lyophilized, For solutionIntravenousSagent Pharmaceuticals25021-191

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