What is NDC 68071-2242?

68071-2242 is the product NDC for Ivermectin, Ivermectin 3 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ivermectin?

28 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ivermectin NDC 68071-2242 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-2242Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-2242Add 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
68071-2242-3	6807122420368071224203	2 BLISTER PACK in 1 CARTON (68071-2242-3) / 10 TABLET in 1 BLISTER PACKMarketed from Nov 15, 2014

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): Ivermectin
Generic name (nonproprietary): ivermectin
Active ingredients: Ivermectin — 3 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204154
Marketing start: Nov 15, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 68071-2242_1d76541f-80d8-2a55-e063-6294a90aa5f9SPL ID 1d76541f-80d8-2a55-e063-6294a90aa5f9SPL set ID ad6539f2-94de-1bc5-e053-2a95a90a4cf2RxCUI 311207UNII 8883YP2R6DUPC 0368071224238
Pharmacologic class: Antiparasitic; Pediculicide

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

N468071224203 followed by a unit qualifier and the quantity

Package 68071-2242-03. 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 Jul 17, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Ivermectin is indicated for the treatment of the following infections: Strongyloidiasis of the intestinal tract Ivermectin is indicated for the treatment of intestinal (i.e., nondisseminated) strongyloidiasis due to the nematode parasite Strongyloides stercoralis . This indication is based on clinical studies of both comparative and open-label designs, in which 64-100% of infected patients were cured following a single 200-mcg/kg dose of ivermectin (See CLINICAL PHARMACOLOGY, Clinical Studies ). Onchocerciasis Ivermectin is indicated for the treatment of onchocerciasis due to the nematode parasite Onchocerca volvulus . This indication is based on randomized, double-blin…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-2242

What is NDC 68071-2242?: 68071-2242 is the product NDC for Ivermectin, Ivermectin 3 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ivermectin.
What is the active ingredient?: Ivermectin.
Who is the labeler?: NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ivermectin?: 28 other product NDCs are listed under this name. See all Ivermectin 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 Ivermectin NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ivermectin	Ivermectin 5 mg/g	LotionTopical	Azurity Pharmaceuticals, Inc.	24338-119	24338-0119-45
Ivermectin	Ivermectin 5 mg/g	LotionTopical	YYBA Corp	73581-021	73581-0021-04
Ivermectin	Ivermectin 3 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-293	27241-0293-73
Ivermectin	Ivermectin 5 mg/g	LotionTopical	AmerisourceBergen	46122-827	46122-0827-36
Ivermectin	Ivermectin 3 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1731	70771-1731-03
Ivermectin	Ivermectin 3 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-223	72578-0223-83
Ivermectin	Ivermectin 5 mg/g	LotionTopical	CVS Pharmacy	51316-985	51316-0985-08
Ivermectin	Ivermectin 3 mg/1	TabletOral	Advagen Pharma Ltd	72888-206	72888-0206-0972888-0206-3072888-0206-66
Ivermectin	Ivermectin 6 mg/1	TabletOral	Advagen Pharma Ltd	72888-207	72888-0207-0972888-0207-3072888-0207-66
ivermectin	Ivermectin 3 mg/1	TabletOral	EPIC PHARMA LLC	42806-017	42806-0017-20

All 29 Ivermectin NDCs

Other NDCs under ANDA 204154

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

FDA NDC Directory listings under ANDA 204154
Product	Strength	Form · route	Labeler	Product NDC
Ivermectin	Ivermectin 3 mg/1	TabletOral	Edenbridge Pharmaceuticals LLC.	42799-806
Ivermectin	Ivermectin 3 mg/1	TabletOral	A-S Medication Solutions	50090-5587
Ivermectin	Ivermectin 3 mg/1	TabletOral	Asclemed USA, Inc.	76420-619