NDC codes

FDA NDC Directory
Product NDC (as listed)82432-103Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82432-0103Add 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
82432-103-01824320103011 VIAL, GLASS in 1 CARTON (82432-103-01) / 10 mL in 1 VIAL, GLASSMarketed from Sep 11, 2024
82432-103-028243201030210 VIAL, GLASS in 1 CARTON (82432-103-02) / 10 mL in 1 VIAL, GLASSMarketed from Nov 17, 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)
Nicardipine Hydrochloride
Generic name (nonproprietary)
nicardipine hydrochloride
Active ingredients
Nicardipine hydrochloride — 25 mg/10mL
Dosage form
Injection
Route
Intravenous
Labeler
Chengdu Shuode Pharmaceutical Co., LtdNDC labeler code 82432
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217548
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Cytochrome P450 2C19 Inhibitors (Mechanism)Cytochrome P450 2C8 Inhibitors (Mechanism)Cytochrome P450 2D6 Inhibitors (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 82432-103_434901d7-2140-d6d8-e063-6394a90a07c4SPL ID 434901d7-2140-d6d8-e063-6394a90a07c4SPL set ID 433dbca3-0a86-44c2-835d-1051c1c93878RxCUI 858607UNII K5BC5011K3
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

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

N482432010301 followed by a unit qualifier and the quantity

Package 82432-0103-01. 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 Nicardipine hydrochloride injection is a calcium channel blocker indicated for the short-term treatment of hypertension when oral therapy is not feasible.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82432-103

What is NDC 82432-103?
82432-103 is the product NDC for Nicardipine Hydrochloride, Nicardipine hydrochloride 25 mg/10mL injection, listed with the FDA by Chengdu Shuode Pharmaceutical Co., Ltd. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nicardipine Hydrochloride.
What is the active ingredient?
Nicardipine hydrochloride.
Who is the labeler?
Chengdu Shuode Pharmaceutical Co., Ltd, NDC labeler code 82432. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nicardipine Hydrochloride?
43 other product NDCs are listed under this name. See all Nicardipine Hydrochloride 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 Nicardipine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Nicardipine HydrochlorideNicardipine hydrochloride .1 mg/mLInjectionIntravenousFresenius Kabi USA, LLC65219-29665219-0296-20
Nicardipine HydrochlorideNicardipine hydrochloride .2 mg/mLInjectionIntravenousFresenius Kabi USA, LLC65219-29865219-0298-20
Nicardipine HydrochlorideNicardipine hydrochloride 20 mg/1CapsuleOralAmerisyn LLC87564-02787564-0027-90
Nicardipine HydrochlorideNicardipine hydrochloride 30 mg/1CapsuleOralAmerisyn LLC87564-02887564-0028-90
Nicardipine HydrochlorideNicardipine hydrochloride .1 mg/mLInjectionIntravenousCaplin Steriles Limited65145-19765145-0197-10
Nicardipine HydrochlorideNicardipine hydrochloride .2 mg/mLInjectionIntravenousCaplin Steriles Limited65145-19865145-0198-10
Nicardipine HydrochlorideNicardipine hydrochloride .1 mg/mLInjectionIntravenousSomerset Therapeutics, LLC70069-87570069-0875-10
Nicardipine HydrochlorideNicardipine hydrochloride .2 mg/mLInjectionIntravenousSomerset Therapeutics, LLC70069-87670069-0876-10
Nicardipine hydrochlorideNicardipine hydrochloride 2.5 mg/mLInjectionIntravenousLifestar Pharma LLC70756-68670756-0686-10
Nicardipine HydrochlorideNicardipine hydrochloride 20 mg/1CapsuleOralAmici Pharma Inc69292-62069292-0620-90

All 44 Nicardipine Hydrochloride NDCs

Other NDCs under ANDA 217548

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

FDA NDC Directory listings under ANDA 217548
ProductStrengthForm · routeLabelerProduct NDC
Nicardipine HydrochlorideNicardipine hydrochloride 25 mg/10mLInjectionIntravenousFresenius Kabi USA, LLC65219-818

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