What is NDC 65841-743?

65841-743 is the product NDC for Anastrozole, Anastrozole 1 mg/1 tablet, coated, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 65841. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Anastrozole?

38 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Anastrozole NDC 65841-743 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)65841-743Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65841-0743Add 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 NDC	11-digit (billing)	Package	Copy
65841-743-06	6584107430665841074306	30 TABLET, COATED in 1 BOTTLE (65841-743-06)Marketed from Jun 27, 2010
65841-743-10	6584107431065841074310	1000 TABLET, COATED in 1 BOTTLE (65841-743-10)Marketed from Jun 27, 2010

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): Anastrozole
Generic name (nonproprietary): anastrozole
Active ingredients: Anastrozole — 1 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 65841
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078921
Marketing start: Jun 27, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Aromatase Inhibitors (Mechanism)
Identifiers: Product ID 65841-743_756f0274-e970-4317-92c0-f5005b5bf9f3SPL ID 756f0274-e970-4317-92c0-f5005b5bf9f3SPL set ID 965c4cb1-f6b8-47ac-bf13-c36639aa908fRxCUI 199224UNII 2Z07MYW1AZ
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

N465841074306 followed by a unit qualifier and the quantity

Package 65841-0743-06. 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 Nov 25, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 65841-743

What is NDC 65841-743?: 65841-743 is the product NDC for Anastrozole, Anastrozole 1 mg/1 tablet, coated, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Anastrozole.
What is the active ingredient?: Anastrozole.
Who is the labeler?: Zydus Lifesciences Limited, NDC labeler code 65841. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Anastrozole?: 38 other product NDCs are listed under this name. See all Anastrozole 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 Anastrozole NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Anastrozole	Anastrozole 1 mg/1	TabletOral	Direct_Rx	72189-682	72189-0682-30
Anastrozole	Anastrozole 1 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-575	72789-0575-1572789-0575-30
Anastrozoleanastrozole tablets	Anastrozole 1 mg/1	TabletOral	Upsher-Smith Laboratories, LLC	24979-725	24979-0725-0624979-0725-07
Anastrozole	Anastrozole 1 mg/1	TabletOral	AvKARE	42291-016	42291-0016-3042291-0016-90
Anastrozole	Anastrozole 1 mg/1	TabletOral	Direct_Rx	72189-415	72189-0415-30
Anastrozole	Anastrozole 1 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-236	59651-0236-3059651-0236-90
Anastrozole	Anastrozole 1 mg/1	Tablet, Film coatedOral	AvKARE	42291-085	42291-0085-3042291-0085-90
Anastrozole	Anastrozole 1 mg/1	TabletOral	AvPAK	50268-075	50268-0075-15
Anastrozoleanastrozole tablets	Anastrozole 1 mg/1	TabletOral	Avet Pharmaceuticals Inc	23155-857	23155-0857-0323155-0857-0523155-0857-09
Anastrozole	Anastrozole 1 mg/1	TabletOral	Chartwell RX, LLC	62135-490	62135-0490-3062135-0490-90

All 39 Anastrozole NDCs

Other NDCs under ANDA 078921

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

FDA NDC Directory listings under ANDA 078921
Product	Strength	Form · route	Labeler	Product NDC
Anastrozole	Anastrozole 1 mg/1	Tablet, CoatedOral	American Health Packaging	60687-112
Anastrozole	Anastrozole 1 mg/1	Tablet, CoatedOral	BluePoint Laboratories	68001-155
Anastrozole	Anastrozole 1 mg/1	Tablet, CoatedOral	Zydus Pharmaceuticals USA Inc.	68382-209
Anastrozole	Anastrozole 1 mg/1	Tablet, CoatedOral	Bryant Ranch Prepack	71335-3145
Anastrozole	Anastrozole 1 mg/1	Tablet, CoatedOral	PD-Rx Pharmaceuticals, Inc.	72789-342