methocarbamol

Generic: methocarbamol

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8507
Product ID 0615-8507_ae34b391-aa06-4b23-b834-27718ed65757
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213967
Listing Expiration 2026-12-31
Marketing Start 2020-08-12

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 06158507
Hyphenated Format 0615-8507

Supplemental Identifiers

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

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8507-39)
source: ndc

Packages (1)

0615-8507-39 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8507-39)

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": "ae34b391-aa06-4b23-b834-27718ed65757", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["32ea8117-4a35-4e2c-93bc-866544b2c3be"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8507-39)", "package_ndc": "0615-8507-39", "marketing_start_date": "20240312"}], "brand_name": "Methocarbamol", "product_id": "0615-8507_ae34b391-aa06-4b23-b834-27718ed65757", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "0615-8507", "generic_name": "Methocarbamol", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA213967", "marketing_category": "ANDA", "marketing_start_date": "20200812", "listing_expiration_date": "20261231"}