What is NDC 87564-054?

87564-054 is the product NDC for Mexiletine Hydrochloride, Mexiletine hydrochloride 250 mg/1 capsule, listed with the FDA by Amerisyn LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Amerisyn LLC, NDC labeler code 87564. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Mexiletine Hydrochloride?

47 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Mexiletine Hydrochloride NDC 87564-054

NDC codes

FDA NDC Directory

Product NDC (as listed)87564-054Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87564-0054Add 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
87564-054-10	8756400541087564005410	100 CAPSULE in 1 BOTTLE (87564-054-10)Marketed from Aug 6, 2026

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): Mexiletine Hydrochloride
Generic name (nonproprietary): mexiletine hydrochloride
Active ingredients: Mexiletine hydrochloride — 250 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Amerisyn LLCNDC labeler code 87564
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214089
Marketing start: Aug 6, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 87564-054_58b7a829-14a7-2e0a-e063-6394a90a23a6SPL ID 58b7a829-14a7-2e0a-e063-6394a90a23a6SPL set ID 58b7a7f5-5ae0-2f60-e063-6394a90a37ddRxCUI 1362706, 1362712, 1362720UNII 606D60IS38UPC 0387564053100, 0387564054107, 0387564052103
Pharmacologic class: Antiarrhythmic

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

N487564005410 followed by a unit qualifier and the quantity

Package 87564-0054-10. 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 Aug 10, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Mexiletine hydrochloride capsules, USP are indicated for the treatment of documented ventricular arrhythmias, such as sustained ventricular tachycardia, that, in the judgment of the physician, are life-threatening. Because of the proarrhythmic effects of mexiletine, its use with lesser arrhythmias is generally not recommended. Treatment of patients with asymptomatic ventricular premature contractions should be avoided. Initiation of mexiletine treatment, as with other antiarrhythmic agents used to treat life-threatening arrhythmias, should be carried out in the hospital. Antiarrhythmic drugs have not been shown to enhance survival in patients with ventricular arrhythmia…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87564-054

What is NDC 87564-054?: 87564-054 is the product NDC for Mexiletine Hydrochloride, Mexiletine hydrochloride 250 mg/1 capsule, listed with the FDA by Amerisyn LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mexiletine Hydrochloride.
What is the active ingredient?: Mexiletine hydrochloride.
Who is the labeler?: Amerisyn LLC, NDC labeler code 87564. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mexiletine Hydrochloride?: 47 other product NDCs are listed under this name. See all Mexiletine 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 Mexiletine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Amerisyn LLC	87564-052	87564-0052-10
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Amerisyn LLC	87564-053	87564-0053-10
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Macleods Pharmaceuticals Limited	33342-555	33342-0555-1133342-0555-12
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Macleods Pharmaceuticals Limited	33342-556	33342-0556-1133342-0556-12
Mexiletine Hydrochloride	Mexiletine hydrochloride 250 mg/1	CapsuleOral	Macleods Pharmaceuticals Limited	33342-557	33342-0557-1133342-0557-12
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Rising Pharma Holdings, Inc.	64980-666	64980-0666-01
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Rising Pharma Holdings, Inc.	64980-667	64980-0667-01
Mexiletine Hydrochloride	Mexiletine hydrochloride 250 mg/1	CapsuleOral	Rising Pharma Holdings, Inc.	64980-668	64980-0668-01
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-3171	71335-3171-0171335-3171-02
Mexiletine hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	American Health Packaging	60687-778	60687-0778-21

All 48 Mexiletine Hydrochloride NDCs

Other NDCs under ANDA 214089

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

FDA NDC Directory listings under ANDA 214089
Product	Strength	Form · route	Labeler	Product NDC
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	62756-955
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	62756-956
Mexiletine Hydrochloride	Mexiletine hydrochloride 250 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	62756-957
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-9179
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-9180
Mexiletine Hydrochloride	Mexiletine hydrochloride 250 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-9181
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2922
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2928
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-1782
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-1783
Mexiletine Hydrochloride	Mexiletine hydrochloride 250 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-1784
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Senores Pharmaceuticals, Inc.	82012-028
Mexiletine Hydrochloride	Mexiletine hydrochloride 250 mg/1	CapsuleOral	Senores Pharmaceuticals, Inc.	82012-029
Mexiletine Hydrochloride	Mexiletine hydrochloride 150 mg/1	CapsuleOral	Amerisyn LLC	87564-052
Mexiletine Hydrochloride	Mexiletine hydrochloride 200 mg/1	CapsuleOral	Amerisyn LLC	87564-053