metaxalone

Generic: metaxalone

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metaxalone
Generic Name metaxalone
Labeler amneal pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metaxalone 800 mg/1

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 65162-553
Product ID 65162-553_5dbbcb1c-6935-4264-a95c-36d5555afc6c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203399
Listing Expiration 2026-12-31
Marketing Start 2013-05-31

Pharmacologic Class

Established (EPC)
muscle relaxant [epc]
Physiologic Effect
centrally-mediated muscle relaxation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65162553
Hyphenated Format 65162-553

Supplemental Identifiers

RxCUI
351254
UPC
0365162553109
UNII
1NMA9J598Y
NUI
N0000175730 N0000175737

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name metaxalone (source: ndc)
Generic Name metaxalone (source: ndc)
Application Number ANDA203399 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (65162-553-10)
  • 500 TABLET in 1 BOTTLE (65162-553-50)
source: ndc

Packages (2)

Ingredients (1)

metaxalone (800 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5dbbcb1c-6935-4264-a95c-36d5555afc6c", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0365162553109"], "unii": ["1NMA9J598Y"], "rxcui": ["351254"], "spl_set_id": ["3aa9dba9-29b0-4520-a0f7-66d19d52c6bc"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-553-10)", "package_ndc": "65162-553-10", "marketing_start_date": "20130531"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-553-50)", "package_ndc": "65162-553-50", "marketing_start_date": "20130531"}], "brand_name": "Metaxalone", "product_id": "65162-553_5dbbcb1c-6935-4264-a95c-36d5555afc6c", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "65162-553", "generic_name": "Metaxalone", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metaxalone", "active_ingredients": [{"name": "METAXALONE", "strength": "800 mg/1"}], "application_number": "ANDA203399", "marketing_category": "ANDA", "marketing_start_date": "20130531", "listing_expiration_date": "20261231"}