metaxalone

Generic: metaxalone

Labeler: cipla usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metaxalone
Generic Name metaxalone
Labeler cipla usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metaxalone 400 mg/1

Manufacturer
CIPLA USA INC.

Identifiers & Regulatory

Product NDC 69097-998
Product ID 69097-998_ab6ad4e1-6b03-45c9-b4d0-59bda8e3b35d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207466
Listing Expiration 2026-12-31
Marketing Start 2023-06-12

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 69097998
Hyphenated Format 69097-998

Supplemental Identifiers

RxCUI
197935
UPC
0369097998073
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 ANDA207466 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69097-998-07)
source: ndc

Packages (1)

Ingredients (1)

metaxalone (400 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ab6ad4e1-6b03-45c9-b4d0-59bda8e3b35d", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0369097998073"], "unii": ["1NMA9J598Y"], "rxcui": ["197935"], "spl_set_id": ["c1f49112-e8ce-43a9-bdb8-1a3db4fb6bc4"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["CIPLA USA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69097-998-07)", "package_ndc": "69097-998-07", "marketing_start_date": "20230612"}], "brand_name": "Metaxalone", "product_id": "69097-998_ab6ad4e1-6b03-45c9-b4d0-59bda8e3b35d", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "69097-998", "generic_name": "Metaxalone", "labeler_name": "CIPLA USA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metaxalone", "active_ingredients": [{"name": "METAXALONE", "strength": "400 mg/1"}], "application_number": "ANDA207466", "marketing_category": "ANDA", "marketing_start_date": "20230612", "listing_expiration_date": "20261231"}