methocarbamol

Generic: methocarbamol

Labeler: advanced rx pharmacy of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler advanced rx pharmacy of tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0283
Product ID 80425-0283_2a9ba8f4-6ceb-e827-e063-6394a90a0300
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040489
Listing Expiration 2026-12-31
Marketing Start 2023-03-07

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 804250283
Hyphenated Format 80425-0283

Supplemental Identifiers

RxCUI
197943
UNII
125OD7737X
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 methocarbamol (source: ndc)
Generic Name methocarbamol (source: ndc)
Application Number ANDA040489 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (80425-0283-1)
  • 60 TABLET in 1 BOTTLE (80425-0283-2)
  • 90 TABLET in 1 BOTTLE (80425-0283-3)
  • 120 TABLET in 1 BOTTLE (80425-0283-4)
  • 180 TABLET in 1 BOTTLE (80425-0283-5)
source: ndc

Packages (5)

80425-0283-1 30 TABLET in 1 BOTTLE (80425-0283-1) 80425-0283-2 60 TABLET in 1 BOTTLE (80425-0283-2) 80425-0283-3 90 TABLET in 1 BOTTLE (80425-0283-3) 80425-0283-4 120 TABLET in 1 BOTTLE (80425-0283-4) 80425-0283-5 180 TABLET in 1 BOTTLE (80425-0283-5)

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": "2a9ba8f4-6ceb-e827-e063-6394a90a0300", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["f6567e04-12f0-fa79-e053-2995a90a9a0e"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0283-1)", "package_ndc": "80425-0283-1", "marketing_start_date": "20230307"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0283-2)", "package_ndc": "80425-0283-2", "marketing_start_date": "20230307"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0283-3)", "package_ndc": "80425-0283-3", "marketing_start_date": "20230307"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (80425-0283-4)", "package_ndc": "80425-0283-4", "marketing_start_date": "20230307"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (80425-0283-5)", "package_ndc": "80425-0283-5", "marketing_start_date": "20230307"}], "brand_name": "Methocarbamol", "product_id": "80425-0283_2a9ba8f4-6ceb-e827-e063-6394a90a0300", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "80425-0283", "generic_name": "Methocarbamol", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20230307", "listing_expiration_date": "20261231"}