Nicardipine Hydrochloride NDC 24658-750

NDC codes

FDA NDC Directory

Product NDC (as listed)24658-750Labeler and product segments. Claims need a package NDC.

Product NDC at billing width24658-0750Add 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 NDC	11-digit (billing)	Package	Copy
24658-750-90	24658075090	90 CAPSULE in 1 BOTTLE (24658-750-90)Marketed from Dec 15, 2016

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 — 20 mg/1
Dosage form: Capsule
Route: Oral
Labeler: PuraCap Laboratories LLC dba Blu Pharmaceuticals
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074928
Marketing start: Dec 15, 2016
Listing expires: Dec 31, 2026
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 24658-750_69c60be8-143d-4a50-8a66-46c01c416372SPL ID 69c60be8-143d-4a50-8a66-46c01c416372SPL set ID 065efabf-8c7d-4dd5-aef2-700c2eca399dRxCUI 858613, 858616UNII K5BC5011K3UPC 0324658750903, 0324658751900
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 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

N424658075090 followed by a unit qualifier and the quantity

Package 24658-0750-90. 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 Jan 7, 2019.

Indications (excerpt from the label)

INDICATIONS AND USAGE I. Stable Angina Nicardipine hydrochloride capsules are indicated for the management of patients with chronic stable angina (effort-associated angina). Nicardipine hydrochloride capsules may be used alone or in combination with beta-blockers. II. Hypertension Nicardipine hydrochloride capsules are indicated for the treatment of hypertension. Nicardipine hydrochloride capsules may be used alone or in combination with other antihypertensive drugs. In administering nicardipine hydrochloride it is important to be aware of the relatively large peak to trough differences in blood pressure effect (See DOSAGE AND ADMINISTRATION ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 074928

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

FDA NDC Directory listings under ANDA 074928
Product	Strength	Form · route	Labeler	Product NDC
Nicardipine Hydrochloride	Nicardipine hydrochloride 20 mg/1	CapsuleOral	Epic Pharma, LLC	42806-501
Nicardipine Hydrochloride	Nicardipine hydrochloride 30 mg/1	CapsuleOral	Epic Pharma, LLC	42806-502
Nicardipine Hydrochloride	Nicardipine hydrochloride 30 mg/1	CapsuleOral	PuraCap Laboratories LLC dba Blu Pharmaceuticals	24658-751