NDC codes

FDA NDC Directory
Product NDC (as listed)60687-309Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0309Add 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
60687-309-216068703092130 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-309-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-309-11)Marketed from Feb 15, 2018

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)
Linezolid
Generic name (nonproprietary)
linezolid
Active ingredients
Linezolid — 600 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204239
Marketing start
Listing expires
Other FDA classes
Oxazolidinones (Chemical structure)
Identifiers
Product ID 60687-309_278685f1-7b24-ea7e-e063-6394a90a9713SPL ID 278685f1-7b24-ea7e-e063-6394a90a9713SPL set ID bc12bd87-5ef0-4ebe-bc00-cbd7896ce08cRxCUI 311347UNII ISQ9I6J12J
Pharmacologic class
Oxazolidinone Antibacterial

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

N460687030921 followed by a unit qualifier and the quantity

Package 60687-0309-21. 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 .

Indications (excerpt from the label)

Linezolid is an oxazolidinone-class antibacterial indicated in adults for the treatment of the following infections caused by susceptible Gram-positive bacteria: Nosocomial pneumonia (1.1) ; Community-acquired pneumonia (1.2) ; Complicated skin and skin structure infections, including diabetic foot infections, without concomitant osteomyelitis (1.3) ; Uncomplicated skin and skin structure infections (1.4) ; Vancomycin-resistant Enterococcus faecium infections. (1.5) Limitations of Use (1.6) : Linezolid tablets are not indicated for the treatment of Gram-negative infections. The safety and efficacy of linezolid formulations given for longer than 28 days have not been evaluated in controlled c…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-309

What is NDC 60687-309?
60687-309 is the product NDC for Linezolid, Linezolid 600 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Linezolid.
What is the active ingredient?
Linezolid.
Who is the labeler?
American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Linezolid?
32 other product NDCs are listed under this name. See all Linezolid 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 Linezolid NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LinezolidLinezolid 600 mg/300mLInjection, SolutionIntravenousCaplin Steriles Limited65145-18165145-0181-10
LinezolidLinezolid 600 mg/1Tablet, Film coatedOralCoupler LLC67046-157667046-1576-03
LinezolidLinezolid 600 mg/1Tablet, CoatedOralMacleods Pharmaceuticals Limited33342-35233342-0352-0633342-0352-1133342-0352-31+1 more
LinezolidLinezolid 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-403470518-4034-0070518-4034-01
LinezolidLinezolid 600 mg/300mLInjection, SolutionIntravenousPiramal Critical Care Inc66794-21966794-0219-43
LinezolidLinezolid 600 mg/300mLInjectionIntravenousPiramal Critical Care Inc.66794-23666794-0236-43
LinezolidLinezolid 600 mg/1TabletOralRising Pharma Holdings, Inc.64980-56164980-0561-0264980-0561-03
LinezolidLinezolid 600 mg/1TabletOralSportpharm LLC85766-07585766-0075-2085766-0075-30
LinezolidLinezolid 100 mg/5mLGranule, For suspensionOralAmerican Health Packaging60687-75460687-0754-05
LinezolidLinezolid 600 mg/300mLInjection, SolutionIntravenousHikma Pharmaceuticals USA Inc.0143-953400143-9534-10

All 33 Linezolid NDCs

Other NDCs under ANDA 204239

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

FDA NDC Directory listings under ANDA 204239
ProductStrengthForm · routeLabelerProduct NDC
LinezolidLinezolid 600 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-749
LinezolidLinezolid 600 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-8576
LinezolidLinezolid 600 mg/1Tablet, Film coatedOralCoupler LLC67046-1576

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