NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1731Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1731Add 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 NDC11-digit (billing)PackageCopy
70771-1731-3707711731032 BLISTER PACK in 1 CARTON (70771-1731-3) / 10 TABLET in 1 BLISTER PACK (70771-1731-2)Marketed from Feb 27, 2026

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
Ivermectin3 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216863
Marketing start
Listing expires
Identifiers
Product ID 70771-1731_865fe6e0-775f-439c-97d3-762298423d78SPL ID 865fe6e0-775f-439c-97d3-762298423d78SPL set ID 6d626814-5288-441c-9508-f7f5130fecebRxCUI 311207UNII 8883YP2R6D
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

N470771173103 followed by a unit qualifier and the quantity

Package 70771-1731-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 216863

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

FDA NDC Directory listings under ANDA 216863
ProductStrengthForm · routeLabelerProduct NDC
IvermectinIvermectin 3 mg/1TabletOralViona Pharmaceuticals Inc72578-223

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