What is NDC 72205-051?

72205-051 is the product NDC for Albendazole, Albendazole 200 mg/1 tablet, listed with the FDA by Novadoz Pharmaceuticals LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Novadoz Pharmaceuticals LLC, NDC labeler code 72205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Albendazole?

8 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Albendazole NDC 72205-051 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72205-051Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72205-0051Add 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
72205-051-08	72205005108	2 TABLET in 1 BOTTLE (72205-051-08)Marketed from Feb 24, 2021
72205-051-28	72205005128	28 TABLET in 1 BOTTLE (72205-051-28)Marketed from Feb 24, 2021

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): Albendazole
Generic name (nonproprietary): albendazole
Active ingredients: Albendazole — 200 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Novadoz Pharmaceuticals LLCNDC labeler code 72205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213435
Marketing start: Feb 24, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Cytochrome P450 1A Inducers (Mechanism)
Identifiers: Product ID 72205-051_594f7aab-b336-4d6d-b702-a33346c69645SPL ID 594f7aab-b336-4d6d-b702-a33346c69645SPL set ID 594f7aab-b336-4d6d-b702-a33346c69645RxCUI 199672UNII F4216019LNUPC 0372205051089, 0372205051287
Pharmacologic class: Anthelmintic

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

N472205005108 followed by a unit qualifier and the quantity

Package 72205-0051-08. 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 Feb 1, 2020.

Indications (excerpt from the label)

Albendazole tablet is an anthelmintic drug indicated for: Treatment of parenchymal neurocysticercosis due to active lesions caused by larval forms of the pork tapeworm, Taenia solium . ( 1.1 ) Treatment of cystic hydatid disease of the liver, lung, and peritoneum, caused by the larval form of the dog tapeworm, Echinococcus granulosus . ( 1.2 ) 1.1 Neurocysticercosis Albendazole tablets are indicated for the treatment of parenchymal neurocysticercosis due to active lesions caused by larval forms of the pork tapeworm, Taenia solium . 1.2 Hydatid Disease Albendazole tablets are indicated for the treatment of cystic hydatid disease of the liver, lung, and peritoneum, caused by the larval form of…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72205-051

What is NDC 72205-051?: 72205-051 is the product NDC for Albendazole, Albendazole 200 mg/1 tablet, listed with the FDA by Novadoz Pharmaceuticals LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Albendazole.
What is the active ingredient?: Albendazole.
Who is the labeler?: Novadoz Pharmaceuticals LLC, NDC labeler code 72205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Albendazole?: 8 other product NDCs are listed under this name. See all Albendazole 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 Albendazole NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Albendazole	Albendazole 200 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-681	62332-0681-0262332-0681-28
Albendazole	Albendazole 200 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-681	46708-0681-0246708-0681-28
Albendazole	Albendazole 200 mg/1	TabletOral	Bryant Ranch Prepack	72162-2359	72162-2359-02
Albendazole	Albendazole 200 mg/1	Tablet, Film coatedOral	Dr.Reddys Laboratories Inc	43598-452	43598-0452-0243598-0452-1743598-0452-63
Albendazole	Albendazole 200 mg/1	Tablet, Film coatedOral	Actavis Pharma, Inc.	0591-2712	00591-2712-02
Albendazole	Albendazole 200 mg/1	TabletOral	Edenbridge Pharmaceuticals LLC.	42799-110	42799-0110-02
Albendazole	Albendazole 200 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-258	51407-0258-02
Albendazole	Albendazole 200 mg/1	Tablet, Film coatedOral	Amneal Pharmaceuticals of New York LLC	0115-1701	00115-1701-49

Other NDCs under ANDA 213435

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

FDA NDC Directory listings under ANDA 213435
Product	Strength	Form · route	Labeler	Product NDC
Albendazole	Albendazole 200 mg/1	TabletOral	Bryant Ranch Prepack	72162-2359