methocarbamol

Generic: methocarbamol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3578
Product ID 50090-3578_a527bac5-ad4e-4c49-acda-a457ff2ca164
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208507
Listing Expiration 2026-12-31
Marketing Start 2018-01-15

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 500903578
Hyphenated Format 50090-3578

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 ANDA208507 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-3578-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3578-3)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-3578-4)
source: ndc

Packages (3)

50090-3578-1 20 TABLET, FILM COATED in 1 BOTTLE (50090-3578-1) 50090-3578-3 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3578-3) 50090-3578-4 30 TABLET, FILM COATED in 1 BOTTLE (50090-3578-4)

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": "a527bac5-ad4e-4c49-acda-a457ff2ca164", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["9357672f-5d4d-40f5-a304-e0c34e174dc3"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-3578-1)", "package_ndc": "50090-3578-1", "marketing_start_date": "20180913"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3578-3)", "package_ndc": "50090-3578-3", "marketing_start_date": "20180115"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-3578-4)", "package_ndc": "50090-3578-4", "marketing_start_date": "20190411"}], "brand_name": "Methocarbamol", "product_id": "50090-3578_a527bac5-ad4e-4c49-acda-a457ff2ca164", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-3578", "generic_name": "Methocarbamol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20261231"}