NDC codes

FDA NDC Directory
Product NDC (as listed)60760-093Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60760-0093Add 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
60760-093-206076000932020 TABLET in 1 BOTTLE, PLASTIC (60760-093-20)Marketed from Nov 10, 2017
60760-093-306076000933030 TABLET in 1 BOTTLE, PLASTIC (60760-093-30)Marketed from Nov 10, 2017
60760-093-906076000939090 TABLET in 1 BOTTLE, PLASTIC (60760-093-90)Marketed from Mar 25, 2026

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)
Metaxalone
Generic name (nonproprietary)
metaxalone
Active ingredients
Metaxalone — 800 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203695
Marketing start
Listing expires
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 60760-093_53de4796-3dc4-bbac-e063-6294a90a535aSPL ID 53de4796-3dc4-bbac-e063-6294a90a535aSPL set ID 5de36266-3964-5aca-e053-2991aa0a2205RxCUI 351254UNII 1NMA9J598Y
Pharmacologic class
Muscle Relaxant

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

N460760009320 followed by a unit qualifier and the quantity

Package 60760-0093-20. 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)

Metaxalone tablets are indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults and pediatric patients 13 years of age and older. Metaxalone tablets are a muscle relaxant indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomforts associated with acute, painful musculoskeletal conditions in adults and pediatric patients 13 years of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 203695

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

FDA NDC Directory listings under ANDA 203695
ProductStrengthForm · routeLabelerProduct NDC
MetaxaloneMetaxalone 800 mg/1TabletOralDirect_Rx72189-645
MetaxaloneMetaxalone 800 mg/1TabletOralProficient Rx LP71205-326
MetaxaloneMetaxalone 800 mg/1TabletOralSportpharm LLC85766-011
MetaxaloneMetaxalone 800 mg/1TabletOralBryant Ranch Prepack71335-0375
MetaxaloneMetaxalone 800 mg/1TabletOralPHOENIX RX LLC85509-2341
MetaxaloneMetaxalone 800 mg/1TabletOralBryant Ranch Prepack63629-8014
MetaxaloneMetaxalone 800 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0131
MetaxaloneMetaxalone 800 mg/1TabletOralAsclemed USA, Inc.76420-898
MetaxaloneMetaxalone 800 mg/1TabletOralDoc Rx69306-100
MetaxaloneMetaxalone 800 mg/1TabletOralActavis Pharma, Inc.0591-2341

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