methocarbamol

Generic: methocarbamol

Labeler: trifluent pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler trifluent pharma llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 1000 mg/1

Manufacturer
Trifluent Pharma LLC

Identifiers & Regulatory

Product NDC 73352-510
Product ID 73352-510_e250f07b-f60b-4159-a4c2-7470b7a31c69
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200958
Listing Expiration 2026-12-31
Marketing Start 2025-02-10

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 73352510
Hyphenated Format 73352-510

Supplemental Identifiers

RxCUI
2611794
UPC
0373352510108
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 ANDA200958 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (73352-510-10)
source: ndc

Packages (1)

73352-510-10 100 TABLET, COATED in 1 BOTTLE (73352-510-10)

Ingredients (1)

methocarbamol (1000 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": "e250f07b-f60b-4159-a4c2-7470b7a31c69", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0373352510108"], "unii": ["125OD7737X"], "rxcui": ["2611794"], "spl_set_id": ["de2e3af9-03ab-4dc8-b480-6866474ad1bd"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Trifluent Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (73352-510-10)", "package_ndc": "73352-510-10", "marketing_start_date": "20250210"}], "brand_name": "Methocarbamol", "product_id": "73352-510_e250f07b-f60b-4159-a4c2-7470b7a31c69", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "73352-510", "generic_name": "Methocarbamol", "labeler_name": "Trifluent Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "1000 mg/1"}], "application_number": "ANDA200958", "marketing_category": "ANDA", "marketing_start_date": "20250210", "listing_expiration_date": "20261231"}