Prescription drug · ANDA

ziprasidone NDC 70518-4761

Ziprasidone hydrochloride 20 mg/1 · Capsule · Oral · REMEDYREPACK INC.

NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4761Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4761Add 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
70518-4761-07051847610030 CAPSULE in 1 BLISTER PACK (70518-4761-0)Marketed from Sep 23, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
ziprasidone
Generic name (nonproprietary)
ziprasidone
Active ingredients
Ziprasidone hydrochloride — 20 mg/1
Dosage form
Capsule
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077565
Marketing start
Listing expires
Identifiers
Product ID 70518-4761_5c275cb8-0bf3-9849-e063-6394a90ad300SPL ID 5c275cb8-0bf3-9849-e063-6394a90ad300
Pharmacologic class
Atypical Antipsychotic

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

N470518476100 followed by a unit qualifier and the quantity

Package 70518-4761-00. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70518-4761

What is NDC 70518-4761?
70518-4761 is the product NDC for ziprasidone, Ziprasidone hydrochloride 20 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
ziprasidone.
What is the active ingredient?
Ziprasidone hydrochloride.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for ziprasidone?
19 other product NDCs are listed under this name. See all ziprasidone 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 ziprasidone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ziprasidoneZiprasidone hydrochloride 40 mg/1CapsuleOralREMEDYREPACK INC.70518-471170518-4711-0070518-4711-02
ziprasidoneZiprasidone hydrochloride 80 mg/1CapsuleOralREMEDYREPACK INC.70518-470970518-4709-0070518-4709-0270518-4709-03
ziprasidoneZiprasidone hydrochloride 60 mg/1CapsuleOralREMEDYREPACK INC.70518-447570518-4475-0070518-4475-0170518-4475-03
ziprasidoneZiprasidone hydrochloride 20 mg/1CapsuleOralNorthStar Rx LLC16714-83516714-0835-01
ziprasidoneZiprasidone hydrochloride 40 mg/1CapsuleOralNorthStar Rx LLC16714-83616714-0836-01
ziprasidoneZiprasidone hydrochloride 60 mg/1CapsuleOralNorthStar Rx LLC16714-83716714-0837-01
ziprasidoneZiprasidone hydrochloride 80 mg/1CapsuleOralNorthStar Rx LLC16714-83816714-0838-01
ZiprasidoneZiprasidone hydrochloride 20 mg/1CapsuleOralChartwell RX, LLC62135-99162135-0991-60
ZiprasidoneZiprasidone hydrochloride 40 mg/1CapsuleOralChartwell RX, LLC62135-99262135-0992-60
ZiprasidoneZiprasidone hydrochloride 60 mg/1CapsuleOralChartwell RX, LLC62135-99362135-0993-60

All 20 ziprasidone NDCs

Other NDCs under ANDA 077565

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

FDA NDC Directory listings under ANDA 077565
ProductStrengthForm · routeLabelerProduct NDC
ziprasidone hydrochlorideZiprasidone hydrochloride 20 mg/1CapsuleOralREMEDYREPACK INC.70518-1835
ziprasidone hydrochlorideZiprasidone hydrochloride 60 mg/1CapsuleOralBryant Ranch Prepack71335-9761
ziprasidoneZiprasidone hydrochloride 80 mg/1CapsuleOralREMEDYREPACK INC.70518-4709
ziprasidoneZiprasidone hydrochloride 40 mg/1CapsuleOralREMEDYREPACK INC.70518-4711
ziprasidoneZiprasidone hydrochloride 60 mg/1CapsuleOralREMEDYREPACK INC.70518-4475
ziprasidoneZiprasidone hydrochloride 20 mg/1CapsuleOralNorthStar Rx LLC16714-835
ziprasidoneZiprasidone hydrochloride 40 mg/1CapsuleOralNorthStar Rx LLC16714-836
ziprasidoneZiprasidone hydrochloride 60 mg/1CapsuleOralNorthStar Rx LLC16714-837
ziprasidoneZiprasidone hydrochloride 80 mg/1CapsuleOralNorthStar Rx LLC16714-838
ziprasidoneZiprasidone hydrochloride 20 mg/1CapsuleOralDr. Reddy's Laboratories Limited55111-256
ziprasidoneZiprasidone hydrochloride 40 mg/1CapsuleOralDr. Reddy's Laboratories Limited55111-257
ziprasidoneZiprasidone hydrochloride 60 mg/1CapsuleOralDr. Reddy's Laboratories Limited55111-258
ZiprasidoneZiprasidone hydrochloride 20 mg/1CapsuleOralMajor Pharmaceuticals0904-6269
ziprasidoneZiprasidone hydrochloride 80 mg/1CapsuleOralDr. Reddy's Laboratories Limited55111-259
ziprasidone hydrochlorideZiprasidone hydrochloride 80 mg/1CapsuleOralBryant Ranch Prepack71335-1508
ZiprasidoneZiprasidone hydrochloride 40 mg/1CapsuleOralMajor Pharmaceuticals0904-6270
ZiprasidoneZiprasidone hydrochloride 60 mg/1CapsuleOralMajor Pharmaceuticals0904-6271
ziprasidone hydrochlorideZiprasidone hydrochloride 20 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-3418
ZiprasidoneZiprasidone hydrochloride 80 mg/1CapsuleOralMajor Pharmaceuticals0904-6272
ziprasidone hydrochlorideZiprasidone hydrochloride 40 mg/1CapsuleOralBryant Ranch Prepack71335-2236

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