NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2445Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2445Add 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
72162-2445-172162244501100 TABLET in 1 BOTTLE (72162-2445-1)Marketed from Feb 12, 2025
72162-2445-37216224450330 TABLET in 1 BOTTLE (72162-2445-3)Marketed from Feb 12, 2025

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
Isoniazid — 300 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040090
Marketing start
Listing expires
Identifiers
Product ID 72162-2445_65a61336-06fb-4f1b-8ff1-06a8b0069053SPL ID 65a61336-06fb-4f1b-8ff1-06a8b0069053SPL set ID eeaf09a3-5631-4089-9f17-15750c002e32RxCUI 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

N472162244501 followed by a unit qualifier and the quantity

Package 72162-2445-01. 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)

About NDC 72162-2445

What is NDC 72162-2445?
72162-2445 is the product NDC for isoniazid, Isoniazid 300 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
isoniazid.
What is the active ingredient?
Isoniazid.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for isoniazid?
26 other product NDCs are listed under this name. See all isoniazid 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 isoniazid NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
isoniazidIsoniazid 300 mg/1TabletOralREMEDYREPACK INC.70518-454070518-4540-0070518-4540-01
isoniazidIsoniazid 300 mg/1TabletOralCoupler LLC67046-161767046-1617-03
IsoniazidIsoniazid 300 mg/1TabletOralCoupler LLC67046-157067046-1570-03
IsoniazidIsoniazid 300 mg/1TabletOralREMEDYREPACK INC.70518-431570518-4315-0070518-4315-0170518-4315-02
isoniazidIsoniazid 100 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-80410135-0804-01
isoniazidIsoniazid 300 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-80510135-0805-0110135-0805-30
IsoniazidIsoniazid 300 mg/1TabletOralBryant Ranch Prepack71335-280071335-2800-0171335-2800-0271335-2800-03+2 more
IsoniazidIsoniazid 100 mg/1TabletOralBryant Ranch Prepack71335-308371335-3083-01
IsoniazidIsoniazid 100 mg/1TabletOralGenus Lifesciences64950-21664950-0216-10
IsoniazidIsoniazid 300 mg/1TabletOralGenus Lifesciences64950-21764950-0217-0364950-0217-10

All 27 isoniazid NDCs

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 100 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-804
isoniazidIsoniazid 300 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-805
isoniazidIsoniazid 100 mg/1TabletOralBryant Ranch Prepack72162-2444
isoniazidIsoniazid 300 mg/1TabletOralA-S Medication Solutions50090-7660
isoniazidIsoniazid 300 mg/1TabletOralREMEDYREPACK INC.70518-4540
isoniazidIsoniazid 100 mg/1TabletOralOMNIVIUM PHARMACEUTICALS LLC.81665-107
isoniazidIsoniazid 300 mg/1TabletOralOMNIVIUM PHARMACEUTICALS LLC.81665-108
isoniazidIsoniazid 300 mg/1TabletOralCoupler LLC67046-1617

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