NDC codes

FDA NDC Directory
Product NDC (as listed)71288-029Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71288-0029Add 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
71288-029-11712880029117128800291110 VIAL, SINGLE-DOSE in 1 CARTON (71288-029-11) / 5 mL in 1 VIAL, SINGLE-DOSE (71288-029-10)Marketed from Sep 28, 2022
71288-029-1271288002912712880029121 VIAL, SINGLE-DOSE in 1 CARTON (71288-029-12) / 5 mL in 1 VIAL, SINGLE-DOSE (71288-029-10)Marketed from Nov 1, 2024

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 — 100 mg/5mL
Dosage form
Injection, Powder, Lyophilized, For solution
Route
Intravenous
Labeler
Meitheal Pharmaceuticals Inc.NDC labeler code 71288
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215381
Marketing start
Listing expires
Other FDA classes
Lipopeptides (Chemical structure)
Identifiers
Product ID 71288-029_9571440f-2c9b-4281-b907-0d53408d744eSPL ID 9571440f-2c9b-4281-b907-0d53408d744eSPL set ID 579ff093-0359-4e0e-a6ea-2b6adac80bf0RxCUI 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

N471288002911 followed by a unit qualifier and the quantity

Package 71288-0029-11. 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 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 4 months of age and older undergoing hematopoietic stem cell transplantation [see Clinical Studies ( 14.3 )]. Micafungin for Injection is an echinocandin indicated in adult and pediatric patients for ( 1 ): Treatment of Candidemia, Acute Diss…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71288-029

What is NDC 71288-029?
71288-029 is the product NDC for Micafungin (micafungin sodium), Micafungin sodium 100 mg/5mL injection, powder, lyophilized, for solution, listed with the FDA by Meitheal Pharmaceuticals Inc.. It has 2 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?
Meitheal Pharmaceuticals Inc., NDC labeler code 71288. 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?
19 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 20 Micafungin NDCs

Other NDCs under ANDA 215381

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

FDA NDC Directory listings under ANDA 215381
ProductStrengthForm · routeLabelerProduct NDC
Micafunginmicafungin sodiumMicafungin sodium 50 mg/5mLInjection, Powder, Lyophilized, For solutionIntravenousMeitheal Pharmaceuticals Inc.71288-028

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