NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0132Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0132Add 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
71335-0132-0713350132007133501320060 TABLET, FILM COATED in 1 BOTTLE (71335-0132-0)Marketed from Apr 3, 2014
71335-0132-1713350132017133501320110 TABLET, FILM COATED in 1 BOTTLE (71335-0132-1)Marketed from Apr 3, 2014
71335-0132-271335013202713350132023 TABLET, FILM COATED in 1 BOTTLE (71335-0132-2)Marketed from Apr 3, 2014
71335-0132-3713350132037133501320330 TABLET, FILM COATED in 1 BOTTLE (71335-0132-3)Marketed from Apr 3, 2014
71335-0132-4713350132047133501320415 TABLET, FILM COATED in 1 BOTTLE (71335-0132-4)Marketed from Apr 3, 2014
71335-0132-571335013205713350132056 TABLET, FILM COATED in 1 BOTTLE (71335-0132-5)Marketed from Apr 3, 2014
71335-0132-671335013206713350132064 TABLET, FILM COATED in 1 BOTTLE (71335-0132-6)Marketed from Apr 3, 2014
71335-0132-7713350132077133501320790 TABLET, FILM COATED in 1 BOTTLE (71335-0132-7)Marketed from Apr 3, 2014
71335-0132-8713350132087133501320812 TABLET, FILM COATED in 1 BOTTLE (71335-0132-8)Marketed from Apr 3, 2014
71335-0132-9713350132097133501320920 TABLET, FILM COATED in 1 BOTTLE (71335-0132-9)Marketed from Apr 3, 2014

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)
Ondansetron
Generic name (nonproprietary)
ondansetron
Active ingredients
Ondansetron hydrochloride — 4 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077851
Marketing start
Listing expires
Other FDA classes
Serotonin 3 Receptor Antagonists (Mechanism)
Identifiers
Product ID 71335-0132_aba5e1a7-a00a-4e76-b0e3-dfbe4179eec0SPL ID aba5e1a7-a00a-4e76-b0e3-dfbe4179eec0SPL set ID f08f56de-8678-4da9-8cae-013a5c393453RxCUI 198052UNII NMH84OZK2B

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

N471335013200 followed by a unit qualifier and the quantity

Package 71335-0132-00. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Ondansetron tablets are indicated for the prevention of nausea and vomiting associated with: • highly emetogenic cancer chemotherapy, including cisplatin greater than or equal to 50 mg/m 2 . • initial and repeat courses of moderately emetogenic cancer chemotherapy. • radiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomen. Ondansetron tablets are also indicated for the prevention of postoperative nausea and/or vomiting. Ondansetron tablets are a 5-HT 3 receptor antagonist indicated for the prevention of: • nausea and vomiting associated with highly emetogenic cancer chemotherapy, including cisplatin ≥50 mg/…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0132

What is NDC 71335-0132?
71335-0132 is the product NDC for Ondansetron, Ondansetron hydrochloride 4 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ondansetron.
What is the active ingredient?
Ondansetron 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 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
OndansetronOndansetron 8 mg/1Tablet, Orally disintegratingOralREMEDYREPACK INC.70518-468570518-4685-00
OndansetronOndansetron 8 mg/1Tablet, Orally disintegratingOralPreferred Pharmaceuticals Inc.68788-413368788-4133-0168788-4133-03
OndansetronOndansetron hydrochloride 4 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-488200121-4882-94
OndansetronOndansetron hydrochloride 4 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-088200121-0882-51
OndansetronOndansetron hydrochloride 2 mg/mLInjectionIntramuscular, IntravenousJVET PHARMACEUTICALS LLC86211-11586211-0115-01
OndansetronOndansetron hydrochloride 4 mg/1TabletOralREMEDYREPACK INC.70518-458870518-4588-00
OndansetronOndansetron hydrochloride 2 mg/mLInjection, SolutionIntramuscular, IntravenousHospira, Inc.0409-227100409-2271-25
OndansetronOndansetron 4 mg/1Tablet, Orally disintegratingOralAvKARE42291-45742291-0457-30
OndansetronOndansetron 8 mg/1Tablet, Orally disintegratingOralAvKARE42291-45842291-0458-30
OndansetronOndansetron 8 mg/1Tablet, Orally disintegratingOralSt. Mary's Medical Park Pharmacy60760-93660760-0936-10

All 191 Ondansetron NDCs

Other NDCs under ANDA 077851

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

FDA NDC Directory listings under ANDA 077851
ProductStrengthForm · routeLabelerProduct NDC
OndansetronOndansetron hydrochloride 4 mg/1TabletOralGolden State Medical Supply, Inc.51407-003
OndansetronOndansetron hydrochloride 8 mg/1TabletOralGolden State Medical Supply, Inc.51407-004
OndansetronOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralProficient Rx LP63187-065
OndansetronOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralProficient Rx LP63187-236
ondansetronondansetron hydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralProficient Rx LP63187-513
OndansetronOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralSun Pharmaceutical Industries, Inc.63304-458
OndansetronOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralSun Pharmaceutical Industries, Inc.63304-459
Ondansetronondansetron tabletsOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralNatco Pharma Limited63850-0003
Ondansetronondansetron tabletsOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralNatco Pharma Limited63850-0004
ondansetronondansetron hydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-170
OndansetronOndansetron hydrochloride 4 mg/1TabletOralNatco Pharma USA LLC69339-171
OndansetronOndansetron hydrochloride 8 mg/1TabletOralNatco Pharma USA LLC69339-172
OndansetronOndansetron hydrochloride 4 mg/1TabletOralREMEDYREPACK INC.70518-4588
ondansetronondansetron hydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0815

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