NDC codes

FDA NDC Directory
Product NDC (as listed)77771-424Labeler and product segments. Claims need a package NDC.
Product NDC at billing width77771-0424Add 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
77771-424-60777710424607777104246060 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (77771-424-60)Marketed from Jun 30, 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)
Ranolazine
Generic name (nonproprietary)
ranolazine
Active ingredients
Ranolazine — 1000 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Labeler
Radha Pharmaceuticals, IncNDC labeler code 77771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211829
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2D6 Inhibitors (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Organic Cation Transporter 2 Inhibitors (Mechanism)P-Glycoprotein Inhibitors (Mechanism)
Identifiers
Product ID 77771-424_2db3da6f-14f6-4c55-ad22-55e475ad9f09SPL ID 2db3da6f-14f6-4c55-ad22-55e475ad9f09SPL set ID 38d2833d-44b8-8d46-e063-6394a90a74d8RxCUI 616749, 728231UNII A6IEZ5M406UPC 0377771424602, 0377771423605
Pharmacologic class
Anti-anginal

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

N477771042460 followed by a unit qualifier and the quantity

Package 77771-0424-60. 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)

Ranolazine extended-release tablets are indicated for the treatment of chronic angina. Ranolazine extended-release tablets may be used with beta-blockers, nitrates, calcium channel blockers, anti-platelet therapy, lipid-lowering therapy, ACE inhibitors, and angiotensin receptor blockers. Ranolazine extended-release tablets are an antianginal indicated for the treatment of chronic angina. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 77771-424

What is NDC 77771-424?
77771-424 is the product NDC for Ranolazine, Ranolazine 1000 mg/1 tablet, film coated, extended release, listed with the FDA by Radha Pharmaceuticals, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ranolazine.
What is the active ingredient?
Ranolazine.
Who is the labeler?
Radha Pharmaceuticals, Inc, NDC labeler code 77771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ranolazine?
51 other product NDCs are listed under this name. See all Ranolazine 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 Ranolazine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
RanolazineRanolazine 500 mg/1Tablet, Extended releaseOralUmedica Laboratories USA Inc.60290-05560290-0055-0160290-0055-03
RanolazineRanolazine 1000 mg/1Tablet, Extended releaseOralUmedica Laboratories USA Inc.60290-05660290-0056-0160290-0056-03
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralTorrent Pharma, Inc.13668-75913668-0759-60
RanolazineRanolazine 1000 mg/1Tablet, Film coated, Extended releaseOralTorrent Pharma, Inc.13668-76013668-0760-60
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralZameer Pharmaceuticals LLC90096-15190096-0151-60
RanolazineRanolazine 1000 mg/1Tablet, Film coated, Extended releaseOralZameer Pharmaceuticals LLC90096-15290096-0152-60
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralRadha Pharmaceuticals, Inc77771-42377771-0423-60
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-97171610-0971-42
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralA2A Integrated Pharmaceuticals73141-02173141-0021-02
RanolazineRanolazine 1000 mg/1Tablet, Film coated, Extended releaseOralA2A Integrated Pharmaceuticals73141-02273141-0022-02

All 52 Ranolazine NDCs

Other NDCs under ANDA 211829

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

FDA NDC Directory listings under ANDA 211829
ProductStrengthForm · routeLabelerProduct NDC
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralScieGen Pharmaceuticals, Inc50228-423
RanolazineRanolazine 1000 mg/1Tablet, Film coated, Extended releaseOralScieGen Pharmaceuticals, Inc50228-424
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralWestminster Pharmaceuticals, LLC69367-293
RanolazineRanolazine 1000 mg/1Tablet, Film coated, Extended releaseOralWestminster Pharmaceuticals, LLC69367-294
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralProficient Rx LP71205-867
RanolazineRanolazine 1000 mg/1Tablet, Film coated, Extended releaseOralProficient Rx LP71205-868
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-971
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralRadha Pharmaceuticals, Inc77771-423
RanolazineRanolazine 500 mg/1Tablet, Film coated, Extended releaseOralProficient Rx LP82804-118

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in