methocarbamol

Generic: methocarbamol

Labeler: xlcare pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler xlcare pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
XLCare Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 72865-234
Product ID 72865-234_10a187fd-d89c-8820-e063-6394a90a510e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090200
Listing Expiration 2026-12-31
Marketing Start 2024-02-02

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 72865234
Hyphenated Format 72865-234

Supplemental Identifiers

RxCUI
197943 197944
UPC
0372865234013 0372865233016
UNII
125OD7737X
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 methocarbamol (source: ndc)
Generic Name methocarbamol (source: ndc)
Application Number ANDA090200 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72865-234-01)
  • 500 TABLET in 1 BOTTLE (72865-234-05)
source: ndc

Packages (2)

72865-234-01 100 TABLET in 1 BOTTLE (72865-234-01) 72865-234-05 500 TABLET in 1 BOTTLE (72865-234-05)

Ingredients (1)

methocarbamol (750 mg/1)

Linked Drug Pages (1)

Methocarbamol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10a187fd-d89c-8820-e063-6394a90a510e", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372865234013", "0372865233016"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["f8bfb5cb-b7d0-4e09-b6bd-97a51d82c991"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["XLCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-234-01)", "package_ndc": "72865-234-01", "marketing_start_date": "20240202"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-234-05)", "package_ndc": "72865-234-05", "marketing_start_date": "20240202"}], "brand_name": "Methocarbamol", "product_id": "72865-234_10a187fd-d89c-8820-e063-6394a90a510e", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72865-234", "generic_name": "Methocarbamol", "labeler_name": "XLCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA090200", "marketing_category": "ANDA", "marketing_start_date": "20240202", "listing_expiration_date": "20261231"}