What is NDC 71335-2236?

71335-2236 is the product NDC for ziprasidone hydrochloride, Ziprasidone hydrochloride 40 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 hydrochloride?

44 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

ziprasidone hydrochloride NDC 71335-2236

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2236Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2236Add 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
71335-2236-1	7133522360171335223601	60 CAPSULE in 1 BOTTLE (71335-2236-1)Marketed from Sep 7, 2023
71335-2236-2	7133522360271335223602	28 CAPSULE in 1 BOTTLE (71335-2236-2)Marketed from Sep 7, 2023
71335-2236-3	7133522360371335223603	30 CAPSULE in 1 BOTTLE (71335-2236-3)Marketed from Sep 7, 2023
71335-2236-4	7133522360471335223604	90 CAPSULE in 1 BOTTLE (71335-2236-4)Marketed from Sep 7, 2023

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 hydrochloride
Generic name (nonproprietary): ziprasidone hydrochloride
Active ingredients: Ziprasidone hydrochloride — 40 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077565
Marketing start: Mar 2, 2012
Listing expires: Dec 31, 2026
Identifiers: Product ID 71335-2236_d61f0a69-f8b3-4cc3-8c88-dc6b1deeed6dSPL ID d61f0a69-f8b3-4cc3-8c88-dc6b1deeed6dSPL set ID 48e6e141-66d3-4eab-b0bf-dfd1d44b4832RxCUI 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

N471335223601 followed by a unit qualifier and the quantity

Package 71335-2236-01. 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 Sep 7, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

Ziprasidone capsules are indicated for the treatment of schizophrenia, as monotherapy for the acute treatment of bipolar manic or mixed episodes, and as an adjunct to lithium or valproate for the maintenance treatment of bipolar disorder. When deciding among the alternative treatments available for the condition needing treatment, the prescriber should consider the finding of ziprasidone’s greater capacity to prolong the QT/QTc interval compared to several other antipsychotic drugs [see Warnings and Precautions ( 5.3 ) ]. Prolongation of the QTc interval is associated in some other drugs with the ability to cause torsade de pointes-type arrhythmia, a potentially fatal polymorphic ventricular…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2236

What is NDC 71335-2236?: 71335-2236 is the product NDC for ziprasidone hydrochloride, Ziprasidone hydrochloride 40 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: ziprasidone hydrochloride.
What is the active ingredient?: Ziprasidone hydrochloride.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. 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 hydrochloride?: 44 other product NDCs are listed under this name. See all ziprasidone 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 ziprasidone hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
ziprasidone hydrochlorideziprasidone hcl	Ziprasidone hydrochloride 80 mg/1	CapsuleOral	AvPAK	50268-814	50268-0814-12
ziprasidone hydrochlorideziprasidone hcl	Ziprasidone hydrochloride 20 mg/1	CapsuleOral	AvPAK	50268-811	50268-0811-12
ziprasidone hydrochlorideziprasidone hcl	Ziprasidone hydrochloride 40 mg/1	CapsuleOral	AvPAK	50268-812	50268-0812-12
ziprasidone hydrochlorideziprasidone hcl	Ziprasidone hydrochloride 60 mg/1	CapsuleOral	AvPAK	50268-813	50268-0813-12
Ziprasidone Hydrochloride	Ziprasidone hydrochloride 40 mg/1	CapsuleOral	BluePoint Laboratories	68001-451	68001-0451-06
Ziprasidone Hydrochloride	Ziprasidone hydrochloride 60 mg/1	CapsuleOral	BluePoint Laboratories	68001-452	68001-0452-06
Ziprasidone Hydrochloride	Ziprasidone hydrochloride 80 mg/1	CapsuleOral	BluePoint Laboratories	68001-453	68001-0453-06
Ziprasidone Hydrochloride	Ziprasidone hydrochloride 20 mg/1	CapsuleOral	BluePoint Laboratories	68001-450	68001-0450-06
Ziprasidone Hydrochloride	Ziprasidone hydrochloride 40 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-0787	70518-0787-0070518-0787-01
Ziprasidone Hydrochloride	Ziprasidone hydrochloride 60 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-0782	70518-0782-0170518-0782-03

All 45 ziprasidone hydrochloride 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
Product	Strength	Form · route	Labeler	Product NDC
Ziprasidone	Ziprasidone hydrochloride 20 mg/1	CapsuleOral	Major Pharmaceuticals	0904-6269
Ziprasidone	Ziprasidone hydrochloride 40 mg/1	CapsuleOral	Major Pharmaceuticals	0904-6270
Ziprasidone	Ziprasidone hydrochloride 60 mg/1	CapsuleOral	Major Pharmaceuticals	0904-6271
Ziprasidone	Ziprasidone hydrochloride 80 mg/1	CapsuleOral	Major Pharmaceuticals	0904-6272
ziprasidone	Ziprasidone hydrochloride 20 mg/1	CapsuleOral	NorthStar Rx LLC	16714-835
ziprasidone	Ziprasidone hydrochloride 40 mg/1	CapsuleOral	NorthStar Rx LLC	16714-836
ziprasidone	Ziprasidone hydrochloride 60 mg/1	CapsuleOral	NorthStar Rx LLC	16714-837
ziprasidone	Ziprasidone hydrochloride 80 mg/1	CapsuleOral	NorthStar Rx LLC	16714-838
ziprasidone	Ziprasidone hydrochloride 20 mg/1	CapsuleOral	Dr. Reddy's Laboratories Limited	55111-256
ziprasidone	Ziprasidone hydrochloride 40 mg/1	CapsuleOral	Dr. Reddy's Laboratories Limited	55111-257
ziprasidone	Ziprasidone hydrochloride 60 mg/1	CapsuleOral	Dr. Reddy's Laboratories Limited	55111-258
ziprasidone	Ziprasidone hydrochloride 80 mg/1	CapsuleOral	Dr. Reddy's Laboratories Limited	55111-259
ziprasidone	Ziprasidone hydrochloride 60 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4475
ziprasidone	Ziprasidone hydrochloride 80 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4709
ziprasidone	Ziprasidone hydrochloride 40 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4711
ziprasidone	Ziprasidone hydrochloride 20 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4761
ziprasidone hydrochloride	Ziprasidone hydrochloride 20 mg/1	CapsuleOral	NuCare Pharmaceuticals,Inc.	68071-3418
ziprasidone hydrochloride	Ziprasidone hydrochloride 80 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-1508
ziprasidone hydrochloride	Ziprasidone hydrochloride 60 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-9761