NDC codes

FDA NDC Directory
Product NDC (as listed)65162-553Labeler and product segments. Claims need a package NDC.
Product NDC at billing width65162-0553Add 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
65162-553-106516205531065162055310100 TABLET in 1 BOTTLE (65162-553-10)Marketed from May 31, 2013
65162-553-506516205535065162055350500 TABLET in 1 BOTTLE (65162-553-50)Marketed from May 31, 2013

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
Labeler
Amneal Pharmaceuticals LLCNDC labeler code 65162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203399
Marketing start
Listing expires
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 65162-553_5dbbcb1c-6935-4264-a95c-36d5555afc6cSPL ID 5dbbcb1c-6935-4264-a95c-36d5555afc6cSPL set ID 3aa9dba9-29b0-4520-a0f7-66d19d52c6bcRxCUI 351254UNII 1NMA9J598YUPC 0365162553109
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

N465162055310 followed by a unit qualifier and the quantity

Package 65162-0553-10. 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 is 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)

About NDC 65162-553

What is NDC 65162-553?
65162-553 is the product NDC for Metaxalone, Metaxalone 800 mg/1 tablet, listed with the FDA by Amneal Pharmaceuticals LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Metaxalone.
What is the active ingredient?
Metaxalone.
Who is the labeler?
Amneal Pharmaceuticals LLC, NDC labeler code 65162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Metaxalone?
62 other product NDCs are listed under this name. See all Metaxalone 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 Metaxalone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
MetaxaloneMetaxalone 400 mg/1TabletOralBlue Heron Pharmaceuticals, LLC85622-95085622-0950-10
MetaxaloneMetaxalone 800 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-416868788-4168-0168788-4168-0368788-4168-06+2 more
MetaxaloneMetaxalone 800 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-058080425-0580-0180425-0580-0280425-0580-03
MetaxaloneMetaxalone 800 mg/1TabletOralAvKARE42291-98542291-0985-50
MetaxaloneMetaxalone 800 mg/1TabletOralAvKARE42291-98542291-0985-01
MetaxaloneMetaxalone 800 mg/1TabletOralREMEDYREPACK INC.70518-455970518-4559-0070518-4559-01
MetaxaloneMetaxalone 800 mg/1TabletOralDirect_Rx72189-64572189-0645-3072189-0645-6072189-0645-90
MetaxaloneMetaxalone 800 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-052480425-0524-0180425-0524-0280425-0524-03
MetaxaloneMetaxalone 640 mg/1TabletOralINA Pharmaceutics Inc74157-01874157-0018-60
MetaxaloneMetaxalone 800 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-867868788-8678-0168788-8678-09

All 63 Metaxalone NDCs

Other NDCs under ANDA 203399

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

FDA NDC Directory listings under ANDA 203399
ProductStrengthForm · routeLabelerProduct NDC
MetaxaloneMetaxalone 800 mg/1TabletOralAvKARE42291-985
MetaxaloneMetaxalone 800 mg/1TabletOralAvPAK50268-530
MetaxaloneMetaxalone 800 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-553
MetaxaloneMetaxalone 800 mg/1TabletOralProficient Rx LP63187-490
MetaxaloneMetaxalone 800 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0084

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