methocarbamol

Generic: methocarbamol

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-340
Product ID 59651-340_a67f1603-a117-4a69-b4f2-ea348425396e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213967
Listing Expiration 2026-12-31
Marketing Start 2023-02-09

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 59651340
Hyphenated Format 59651-340

Supplemental Identifiers

RxCUI
197943 197944
UPC
0359651340011
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 ANDA213967 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59651-340-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (59651-340-05)
source: ndc

Packages (2)

59651-340-01 100 TABLET, FILM COATED in 1 BOTTLE (59651-340-01) 59651-340-05 500 TABLET, FILM COATED in 1 BOTTLE (59651-340-05)

Ingredients (1)

methocarbamol (500 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": "a67f1603-a117-4a69-b4f2-ea348425396e", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0359651340011"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["f83dd093-ea53-44c1-a40d-682ebc494b62"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-340-01)", "package_ndc": "59651-340-01", "marketing_start_date": "20230209"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59651-340-05)", "package_ndc": "59651-340-05", "marketing_start_date": "20230209"}], "brand_name": "Methocarbamol", "product_id": "59651-340_a67f1603-a117-4a69-b4f2-ea348425396e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "59651-340", "generic_name": "Methocarbamol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA213967", "marketing_category": "ANDA", "marketing_start_date": "20230209", "listing_expiration_date": "20261231"}