NDC codes

FDA NDC Directory
Product NDC (as listed)0904-6552Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00904-6552Add 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
0904-6552-6100904655261100 BLISTER PACK in 1 CARTON (0904-6552-61) / 1 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Dec 26, 2006

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 hydrochloride
Active ingredients
Ondansetron hydrochloride — 8 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076183
Marketing start
Listing expires
Other FDA classes
Serotonin 3 Receptor Antagonists (Mechanism)
Identifiers
Product ID 0904-6552_c966171f-89bb-402a-b56a-fcc3f43df9f9SPL ID c966171f-89bb-402a-b56a-fcc3f43df9f9SPL set ID a29b5c18-9884-4c88-8827-65d9ad5f69f6RxCUI 198052, 312086UNII 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

N400904655261 followed by a unit qualifier and the quantity

Package 00904-6552-61. 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 076183

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

FDA NDC Directory listings under ANDA 076183
ProductStrengthForm · routeLabelerProduct NDC
ondansetronondansetron hydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-3551
Ondansetronondansetron hydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralDr. Reddy's Laboratories Limited55111-153
Ondansetronondansetron hydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralDr. Reddy's Laboratories Limited55111-154
ondansetron hydrochlorideOndansetron hydrochloride 16 mg/1Tablet, Film coatedOralDr. Reddy's Laboratories Limited55111-155
Ondansetronondansetron hydrochlorideOndansetron hydrochloride 24 mg/1Tablet, Film coatedOralDr. Reddy's Laboratories Limited55111-156
OndansetronOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralHF Acquisition Co LLC, DBA HealthFirst51662-1539
OndansetronOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralHF Acquisition Co LLC, DBA HealthFirst51662-1678
ondansetronondansetron hydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6551
ondansetron hydrochlorideOndansetron hydrochloride 4 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8185
ondansetronondansetron hydrochlorideOndansetron hydrochloride 8 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-7879

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