What is NDC 72664-611?

72664-611 is the product NDC for Leuprolide Acetate kit, listed with the FDA by VGYAAN Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

VGYAAN Pharmaceuticals LLC, NDC labeler code 72664. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Leuprolide Acetate?

11 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Leuprolide Acetate NDC 72664-611 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72664-611Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72664-0611Add 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
72664-611-28	7266406112872664061128	1 KIT in 1 CARTON (72664-611-28) * 2.8 mL in 1 VIAL, MULTI-DOSE * 1 mL in 1 PACKETMarketed from Oct 25, 2020

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): Leuprolide Acetate
Generic name (nonproprietary): leuprolide acetate
Dosage form: Kit
Labeler: VGYAAN Pharmaceuticals LLCNDC labeler code 72664
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213829
Marketing start: Oct 25, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 72664-611_441a43d5-2a8c-2d53-e063-6294a90a385dSPL ID 441a43d5-2a8c-2d53-e063-6294a90a385dSPL set ID bec9077a-3f04-4887-856d-dde2de24584dRxCUI 545835, 797544

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N472664061128 followed by a unit qualifier and the quantity

Package 72664-0611-28. 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.

About NDC 72664-611

What is NDC 72664-611?: 72664-611 is the product NDC for Leuprolide Acetate kit, listed with the FDA by VGYAAN Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Leuprolide Acetate.
Who is the labeler?: VGYAAN Pharmaceuticals LLC, NDC labeler code 72664. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Leuprolide Acetate?: 11 other product NDCs are listed under this name. See all Leuprolide Acetate 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 Leuprolide Acetate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Leuprolide Acetate	Leuprolide acetate 1 mg/.2mL	InjectionSubcutaneous	Endo USA, Inc.	42023-259	42023-0259-00
Leuprolide Acetate	—	Kit	Zydus Pharmaceuticals USA Inc.	70710-1769	70710-1769-03
Leuprolide Acetate	—	Kit	Zydus Lifesciences Limited	70771-1687	70771-1687-03
leuprolide acetate	—	KitSubcutaneous	PAI Holdings, LLC dba PAI Pharma	0121-2106	00121-2106-02
leuprolide acetate	—	KitSubcutaneous	UBI Pharma Inc.	72843-591	72843-0591-99
Leuprolide Acetate	—	KitSubcutaneous	Meitheal Pharmaceuticals Inc	71288-569	71288-0569-90
Leuprolide Acetate	—	KitSubcutaneous	NorthStar RxLLC	72603-344	72603-0344-01
leuprolide acetate	—	KitSubcutaneous	Amneal Pharmaceuticals LLC	70121-2537	70121-2537-06
Leuprolide Acetate	—	Kit	Eugia US LLC	55150-478	55150-0478-01
leuprolide acetate	—	Kit	Sun Pharmaceutical Industries, Inc.	47335-936	47335-0936-40

All 12 Leuprolide Acetate NDCs

Other NDCs under ANDA 213829

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

FDA NDC Directory listings under ANDA 213829
Product	Strength	Form · route	Labeler	Product NDC
Leuprolide Acetate	—	KitSubcutaneous	NorthStar RxLLC	72603-344