NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2396Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2396Add 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
71335-2396-1713352396017133523960130 TABLET, FILM COATED in 1 BOTTLE (71335-2396-1)Marketed from Apr 19, 2024
71335-2396-2713352396027133523960210 TABLET, FILM COATED in 1 BOTTLE (71335-2396-2)Marketed from Jan 3, 2025
71335-2396-3713352396037133523960390 TABLET, FILM COATED in 1 BOTTLE (71335-2396-3)Marketed from Jan 31, 2025
71335-2396-4713352396047133523960440 TABLET, FILM COATED in 1 BOTTLE (71335-2396-4)Marketed from Jan 31, 2025

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)
Letrozole
Generic name (nonproprietary)
letrozole tablets
Active ingredients
Letrozole — 2.5 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 205869
Marketing start
Listing expires
Other FDA classes
Aromatase Inhibitors (Mechanism)
Identifiers
Product ID 71335-2396_77bb27a8-b20e-44eb-b96c-ff1a364a24d1SPL ID 77bb27a8-b20e-44eb-b96c-ff1a364a24d1SPL set ID 6fd92634-c9c5-457e-808c-a4614e8db7dbRxCUI 200064UNII 7LKK855W8I
Pharmacologic class
Aromatase 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

N471335239601 followed by a unit qualifier and the quantity

Package 71335-2396-01. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Letrozole Tablets, USP are aromatase inhibitor indicated for: Adjuvant treatment of postmenopausal women with hormone receptor positive early breast cancer ( 1.1 ) Extended adjuvant treatment of postmenopausal women with early breast cancer who have received prior standard adjuvant tamoxifen therapy ( 1.2 ) First and second-line treatment of postmenopausal women with hormone receptor positive or unknown advanced breast cancer ( 1.3 ) 1.1 Adjuvant Treatment of Early Breast Cancer Letrozole tablets, are indicated for the adjuvant treatment of postmenopausal women with hormone receptor positive early breast cancer. 1.2 Extended Adjuvant Treatment of Early Breast Cancer Letrozole tablets, are in…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2396

What is NDC 71335-2396?
71335-2396 is the product NDC for Letrozole (letrozole tablets), Letrozole 2.5 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Letrozole (Letrozole Tablets).
What is the active ingredient?
Letrozole.
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 Letrozole?
22 other product NDCs are listed under this name. See all Letrozole 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 Letrozole NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LetrozoleLetrozole 2.5 mg/1Tablet, Film coatedOralCarnegie Pharmaceuticals LLC80005-13980005-0139-0880005-0139-10
Letrozoleletrozole tabletsLetrozole 2.5 mg/1Tablet, Film coatedOralUpsher-Smith Laboratories, LLC24979-72624979-0726-07
Letrozoleletrozole tabletsLetrozole 2.5 mg/1Tablet, Film coatedOralAvet Pharmaceuticals Inc.23155-87523155-0875-0323155-0875-0923155-0875-10
LetrozoleLetrozole 2.5 mg/1Tablet, Film coatedOralATLANTIC BIOLOGICALS CORP.17856-003217856-0032-01
LetrozoleLetrozole 2.5 mg/1TabletOralAvPAK50268-47650268-0476-15
Letrozoleletrozole tabletsLetrozole 2.5 mg/1Tablet, Film coatedOralYiling Pharmaceutical, Inc.69117-000469117-0004-01
LetrozoleLetrozole 2.5 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-49162135-0491-3062135-0491-90
LetrozoleLetrozole 2.5 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-18059651-0180-3059651-0180-90
Letrozoleletrozole tabletsLetrozole 2.5 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-98651407-0986-90
LetrozoleLetrozole 2.5 mg/1Tablet, Film coatedOralAvKARE42291-37442291-0374-3042291-0374-90

All 23 Letrozole NDCs

Other NDCs under ANDA 205869

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

FDA NDC Directory listings under ANDA 205869
ProductStrengthForm · routeLabelerProduct NDC
Letrozoleletrozole tabletsLetrozole 2.5 mg/1Tablet, Film coatedOralAvet Pharmaceuticals Inc.23155-875
Letrozoleletrozole tabletsLetrozole 2.5 mg/1Tablet, Film coatedOralUpsher-Smith Laboratories, LLC24979-726
Letrozoleletrozole tabletsLetrozole 2.5 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-986
LetrozoleLetrozole 2.5 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-491
Letrozoleletrozole tabletsLetrozole 2.5 mg/1Tablet, Film coatedOralYiling Pharmaceutical, Inc.69117-0004

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