NDC codes

FDA NDC Directory
Product NDC (as listed)24979-715Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24979-0715Add 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
24979-715-042497907150460 TABLET, FILM COATED in 1 BOTTLE (24979-715-04)Marketed from Dec 1, 2022
24979-715-4424979071544120 TABLET, FILM COATED in 1 BOTTLE (24979-715-44)Marketed from Dec 1, 2022

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)
sorafenib
Generic name (nonproprietary)
sorafenib
Active ingredients
Sorafenib — 200 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209050
Marketing start
Listing expires
Other FDA classes
Protein Kinase Inhibitors (Mechanism)
Identifiers
Product ID 24979-715_55afb5e2-d3ae-6c46-e063-6394a90adec2SPL ID 55afb5e2-d3ae-6c46-e063-6394a90adec2SPL set ID 68aa4b7f-3f13-4e73-b572-aa6c11a8429cRxCUI 597747UNII 9ZOQ3TZI87UPC 0324979715445
Pharmacologic class
Kinase Inhibitor

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

N424979071504 followed by a unit qualifier and the quantity

Package 24979-0715-04. 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)

Sorafenib tablets are a kinase inhibitor indicated for the treatment of Unresectable hepatocellular carcinoma(1.1) Locally recurrent or metastatic, progressive, differentiated thyroid carcinoma (DTC) refractory to radioactive iodine treatment (1.3) 1.1 Hepatocellular Carcinoma Sorafenib tablets are indicated for the treatment of patients with unresectable hepatocellular carcinoma (HCC). 1.3 Differentiated Thyroid Carcinoma Sorafenib tablets are indicated for the treatment of patients with locally recurrent or metastatic, progressive,differentiated thyroid carcinoma (DTC) that is refractory to radioactive iodine treatment.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209050

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

FDA NDC Directory listings under ANDA 209050
ProductStrengthForm · routeLabelerProduct NDC
sorafenibSorafenib 200 mg/1Tablet, Film coatedOralYabao Pharmaceutical Co., Ltd. Beijing51990-201
sorafenibSorafenib 200 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-760

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