What is NDC 43598-452?

43598-452 is the product NDC for Albendazole, Albendazole 200 mg/1 tablet, film coated, listed with the FDA by Dr.Reddys Laboratories Inc. It has 3 package NDCs, shown above in 10- and 11-digit form.

Dr.Reddys Laboratories Inc, NDC labeler code 43598. 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?

7 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 43598-452 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43598-452Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43598-0452Add 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
43598-452-02	4359804520243598045202	2 TABLET, FILM COATED in 1 BOTTLE (43598-452-02)Marketed from Jan 26, 2021
43598-452-17	4359804521743598045217	1 BLISTER PACK in 1 CARTON (43598-452-17) / 8 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Jan 26, 2021
43598-452-63	4359804526343598045263	28 TABLET, FILM COATED in 1 BOTTLE (43598-452-63)Marketed from Jan 26, 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, Film coated
Route: Oral
Labeler: Dr.Reddys Laboratories IncNDC labeler code 43598
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211034
Marketing start: Jan 26, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 1A Inducers (Mechanism)
Identifiers: Product ID 43598-452_370b6498-30f2-48a4-f32a-9ee671cf294eSPL ID 370b6498-30f2-48a4-f32a-9ee671cf294eSPL set ID 9ac95554-94c9-1f38-8f49-ec11979e4ba4RxCUI 199672UNII F4216019LNUPC 0343598452029
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

N443598045202 followed by a unit qualifier and the quantity

Package 43598-0452-02. 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 Jun 10, 2020.

Indications (excerpt from the label)

Albendazole 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 th…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43598-452

What is NDC 43598-452?: 43598-452 is the product NDC for Albendazole, Albendazole 200 mg/1 tablet, film coated, listed with the FDA by Dr.Reddys Laboratories Inc. It has 3 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?: Dr.Reddys Laboratories Inc, NDC labeler code 43598. 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?: 7 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 Limited	46708-681	46708-0681-0246708-0681-28
Albendazole	Albendazole 200 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-681	62332-0681-0262332-0681-28
Albendazole	Albendazole 200 mg/1	TabletOral	Bryant Ranch Prepack	72162-2359	72162-2359-02
Albendazole	Albendazole 200 mg/1	TabletOral	Novadoz Pharmaceuticals LLC	72205-051	72205-0051-0872205-0051-28
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