What is NDC 61919-986?

61919-986 is the product NDC for Ondansetron, Ondansetron 8 mg/1 tablet, orally disintegrating, listed with the FDA by Direct Rx. It has 2 package NDCs, shown above in 10- and 11-digit form.

Direct Rx, NDC labeler code 61919. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ondansetron?

190 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ondansetron NDC 61919-986 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)61919-986Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61919-0986Add 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
61919-986-10	6191909861061919098610	10 TABLET, ORALLY DISINTEGRATING in 1 CARTON (61919-986-10)Marketed from Jan 1, 2014
61919-986-30	6191909863061919098630	30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (61919-986-30)Marketed from Jan 1, 2014

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): Ondansetron
Generic name (nonproprietary): ondansetron
Active ingredients: Ondansetron — 8 mg/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: Direct RxNDC labeler code 61919
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090469
Marketing start: Jan 1, 2014
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin 3 Receptor Antagonists (Mechanism)
Identifiers: Product ID 61919-986_4d3a9354-50c1-c926-e063-6394a90ada40SPL ID 4d3a9354-50c1-c926-e063-6394a90ada40SPL set ID b38feff2-900a-4e0c-8260-8f090edbc0bcRxCUI 312087UNII 4AF302ESOS
Pharmacologic class: Serotonin-3 Receptor Antagonist

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

N461919098610 followed by a unit qualifier and the quantity

Package 61919-0986-10. 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 Mar 17, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy, including cisplatin ≥50 mg/m2. Prevention of nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy. Prevention of nausea and vomiting associated with radiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomen. Prevention of postoperative nausea and/or vomiting. As with other antiemetics, routine prophylaxis is not recommended for patients in whom there is little expectation that nausea and/or vomiting will occur postoperatively. In patients where n…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61919-986

What is NDC 61919-986?: 61919-986 is the product NDC for Ondansetron, Ondansetron 8 mg/1 tablet, orally disintegrating, listed with the FDA by Direct Rx. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ondansetron.
What is the active ingredient?: Ondansetron.
Who is the labeler?: Direct Rx, NDC labeler code 61919. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ondansetron?: 190 other product NDCs are listed under this name. See all Ondansetron 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 Ondansetron NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	REMEDYREPACK INC.	70518-4685	70518-4685-00
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	Preferred Pharmaceuticals Inc.	68788-4133	68788-4133-0168788-4133-03
Ondansetron	Ondansetron hydrochloride 4 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-4882	00121-4882-94
Ondansetron	Ondansetron hydrochloride 4 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0882	00121-0882-51
Ondansetron	Ondansetron hydrochloride 2 mg/mL	InjectionIntramuscular, Intravenous	JVET PHARMACEUTICALS LLC	86211-115	86211-0115-01
Ondansetron	Ondansetron hydrochloride 4 mg/1	TabletOral	REMEDYREPACK INC.	70518-4588	70518-4588-00
Ondansetron	Ondansetron hydrochloride 2 mg/mL	Injection, SolutionIntramuscular, Intravenous	Hospira, Inc.	0409-2271	00409-2271-25
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	AvKARE	42291-457	42291-0457-30
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	AvKARE	42291-458	42291-0458-30
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	St. Mary's Medical Park Pharmacy	60760-936	60760-0936-10

All 191 Ondansetron NDCs

Other NDCs under ANDA 090469

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

FDA NDC Directory listings under ANDA 090469
Product	Strength	Form · route	Labeler	Product NDC
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	Preferred Pharmaceuticals, Inc.	68788-7644
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	NuCare Pharmaceuticals,Inc.	68071-4834
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	Bryant Ranch Prepack	71335-1071
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	Rising Pharma Holdings, Inc.	57237-077
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	Preferred Pharmaceuticals, Inc.	68788-9559
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	Rising Pharma Holdings, Inc.	57237-078
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	NuCare Pharmaceuticals,Inc.	68071-4881
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	Proficient Rx LP	71205-713
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	REMEDYREPACK INC.	70518-1551
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	St. Mary's Medical Park Pharmacy	60760-306
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	PD-Rx Pharmaceuticals, Inc.	43063-857
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	Asclemed USA, Inc.	76420-056
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	Bryant Ranch Prepack	71335-0650
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	Proficient Rx LP	63187-526
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	PD-Rx Pharmaceuticals, Inc.	43063-870
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	Northwind Health Company, LLC	51655-809
Ondansetron ODTondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	Advanced Rx of Tennessee, LLC	80425-0073
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	NuCare Pharmaceuticals,Inc.	68071-2763
Ondansetron	Ondansetron 4 mg/1	Tablet, Orally disintegratingOral	HAWAII REPACK, INC.	85534-0025
Ondansetron	Ondansetron 8 mg/1	Tablet, Orally disintegratingOral	NuCare Pharmaceuticals,Inc.	68071-1730

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