NDC codes

FDA NDC Directory
Product NDC (as listed)68788-9368Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-9368Add 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
68788-9368-1687889368016878893680110 TABLET, FILM COATED in 1 BOTTLE (68788-9368-1)Marketed from Jun 12, 2012
68788-9368-2687889368026878893680212 TABLET, FILM COATED in 1 BOTTLE (68788-9368-2)Marketed from Jun 23, 2017
68788-9368-3687889368036878893680330 TABLET, FILM COATED in 1 BOTTLE (68788-9368-3)Marketed from Jun 12, 2012
68788-9368-5687889368056878893680550 TABLET, FILM COATED in 1 BOTTLE (68788-9368-5)Marketed from Jun 23, 2017

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 Hydrochloride
Generic name (nonproprietary)
ondansetron hydrochloride
Active ingredients
Ondansetron hydrochloride — 4 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Preferred Pharmaceuticals, Inc.NDC labeler code 68788
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078539
Marketing start
Listing expires
Other FDA classes
Serotonin 3 Receptor Antagonists (Mechanism)
Identifiers
Product ID 68788-9368_162d708b-5d8a-4149-a721-a6e5d50ba38fSPL ID 162d708b-5d8a-4149-a721-a6e5d50ba38f

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

N468788936801 followed by a unit qualifier and the quantity

Package 68788-9368-01. 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

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

About NDC 68788-9368

What is NDC 68788-9368?
68788-9368 is the product NDC for Ondansetron Hydrochloride, Ondansetron hydrochloride 4 mg/1 tablet, film coated, listed with the FDA by Preferred Pharmaceuticals, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ondansetron Hydrochloride.
What is the active ingredient?
Ondansetron hydrochloride.
Who is the labeler?
Preferred Pharmaceuticals, Inc., NDC labeler code 68788. 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 Hydrochloride?
76 other product NDCs are listed under this name. See all Ondansetron 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 Ondansetron Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ondansetron hydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralIpca Laboratories Limited83980-01783980-0017-1083980-0017-1383980-0017-97
ondansetron hydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralIpca Laboratories Limited83980-01883980-0018-1083980-0018-1383980-0018-97
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-87860760-0878-10
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-08887441-0088-01
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-06487441-0064-01
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralCoupler LLC67046-124267046-1242-03
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralQuality Care Products, LLC83008-07483008-0074-2083008-0074-30
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-414570518-4145-0070518-4145-0170518-4145-02+3 more
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-865168788-8651-0168788-8651-0268788-8651-03+2 more
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-858268788-8582-0168788-8582-0268788-8582-03+2 more

All 77 Ondansetron Hydrochloride NDCs

Other NDCs under ANDA 078539

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

FDA NDC Directory listings under ANDA 078539
ProductStrengthForm · routeLabelerProduct NDC
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8651
OndansetronOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralPharmPak, Inc.54348-819
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-119
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralPharmpak, Inc.54348-821
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-878
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-9402
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.57237-076
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.57237-075
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-792
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3511
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-034
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralQPharma, Inc.42708-179
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-1585
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralProficient Rx LP71205-744
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1596
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4145
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6342
Ondansetron HydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-813
Ondansetron HydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralRedpharm Drug67296-1562
Ondansetron HCLOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-0072

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