metaxalone

Generic: metaxalone

Labeler: doc rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metaxalone
Generic Name metaxalone
Labeler doc rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metaxalone 800 mg/1

Manufacturer
Doc Rx

Identifiers & Regulatory

Product NDC 69306-311
Product ID 69306-311_db68fb1f-5ead-7808-e053-2995a90a0f27
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204770
Listing Expiration 2026-12-31
Marketing Start 2016-11-22

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 69306311
Hyphenated Format 69306-311

Supplemental Identifiers

RxCUI
351254
UNII
1NMA9J598Y
NUI
N0000175730 N0000175737

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 ANDA204770 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (69306-311-20)
  • 30 TABLET in 1 BOTTLE (69306-311-30)
  • 60 TABLET in 1 BOTTLE (69306-311-60)
  • 90 TABLET in 1 BOTTLE (69306-311-90)
source: ndc

Packages (4)

69306-311-20 20 TABLET in 1 BOTTLE (69306-311-20) 69306-311-30 30 TABLET in 1 BOTTLE (69306-311-30) 69306-311-60 60 TABLET in 1 BOTTLE (69306-311-60) 69306-311-90 90 TABLET in 1 BOTTLE (69306-311-90)

Ingredients (1)

metaxalone (800 mg/1)

Linked Drug Pages (1)

Metaxalone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "db68fb1f-5ead-7808-e053-2995a90a0f27", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["1NMA9J598Y"], "rxcui": ["351254"], "spl_set_id": ["4a558a2f-f9be-40d1-8d02-dd0c8c501ef6"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (69306-311-20)", "package_ndc": "69306-311-20", "marketing_start_date": "20220325"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (69306-311-30)", "package_ndc": "69306-311-30", "marketing_start_date": "20220325"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (69306-311-60)", "package_ndc": "69306-311-60", "marketing_start_date": "20220325"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (69306-311-90)", "package_ndc": "69306-311-90", "marketing_start_date": "20220325"}], "brand_name": "Metaxalone", "product_id": "69306-311_db68fb1f-5ead-7808-e053-2995a90a0f27", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]"], "product_ndc": "69306-311", "generic_name": "Metaxalone", "labeler_name": "Doc Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metaxalone", "active_ingredients": [{"name": "METAXALONE", "strength": "800 mg/1"}], "application_number": "ANDA204770", "marketing_category": "ANDA", "marketing_start_date": "20161122", "listing_expiration_date": "20261231"}