NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4711Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4711Add 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
70518-4711-07051847110050 POUCH in 1 BOX (70518-4711-0) / 1 CAPSULE in 1 POUCH (70518-4711-1)Marketed from Jul 29, 2026
70518-4711-27051847110230 CAPSULE in 1 BLISTER PACK (70518-4711-2)Marketed from Aug 2, 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 hydrochloride40 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077565
Marketing start
Listing expires
Identifiers
Product ID 70518-4711_5823b8b1-cd0d-ea1f-e063-6294a90aee68SPL ID 5823b8b1-cd0d-ea1f-e063-6294a90aee68SPL set ID 6665279a-32ab-43ce-a258-039a6779a1a2RxCUI 313776UNII 216X081ORU
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

N470518471100 followed by a unit qualifier and the quantity

Package 70518-4711-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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

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