NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4540Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4540Add 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
70518-4540-07051845400012 TABLET in 1 BOTTLE, PLASTIC (70518-4540-0)Marketed from Dec 23, 2025
70518-4540-17051845400130 TABLET in 1 BLISTER PACK (70518-4540-1)Marketed from Jan 21, 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)
isoniazid
Generic name (nonproprietary)
isoniazid
Active ingredients
Isoniazid300 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040090
Marketing start
Listing expires
Identifiers
Product ID 70518-4540_5070b8f5-b2f4-8d89-e063-6294a90adf72SPL ID 5070b8f5-b2f4-8d89-e063-6294a90adf72SPL set ID 93252cc8-c8d4-401b-bde5-ca8a3b57651eRxCUI 197832UNII V83O1VOZ8L
Pharmacologic class
Antimycobacterial

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

N470518454000 followed by a unit qualifier and the quantity

Package 70518-4540-00. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Isoniazid is recommended for all forms of tuberculosis in which organisms are susceptible. However, active tuberculosis must be treated with multiple concomitant anti-tuberculosis medications to prevent the emergence of drug resistance. Single-drug treatment of active tuberculosis with isoniazid, or any other medication is inadequate therapy. Isoniazid is recommended as preventive therapy for the following groups, regardless of age. (Note: the criterion for a positive reaction to a skin test (in millimeters of induration) for each group is given in parentheses): 1. Persons with human immunodeficiency virus (HIV) infection (≥ 5 mm) and persons with risk factors for HIV i

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040090

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

FDA NDC Directory listings under ANDA 040090
ProductStrengthForm · routeLabelerProduct NDC
isoniazidIsoniazid 300 mg/1TabletOralA-S Medication Solutions50090-7660
isoniazidIsoniazid 100 mg/1TabletOralBryant Ranch Prepack72162-2444
isoniazidIsoniazid 300 mg/1TabletOralBryant Ranch Prepack72162-2445
isoniazidIsoniazid 100 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-804
isoniazidIsoniazid 300 mg/1TabletOralCoupler LLC67046-1617
isoniazidIsoniazid 300 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-805
isoniazidIsoniazid 100 mg/1TabletOralOMNIVIUM PHARMACEUTICALS LLC.81665-107
isoniazidIsoniazid 300 mg/1TabletOralOMNIVIUM PHARMACEUTICALS LLC.81665-108

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