methocarbamol

Generic: methocarbamol

Labeler: fh2 pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler fh2 pharma llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methocarbamol 1000 mg/1

Manufacturer
FH2 PHARMA LLC

Identifiers & Regulatory

Product NDC 72887-873
Product ID 72887-873_2d7ed9b4-3cba-fb22-e063-6294a90af27a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212707
Listing Expiration 2026-12-31
Marketing Start 2024-08-30

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 72887873
Hyphenated Format 72887-873

Supplemental Identifiers

RxCUI
2611794
UPC
0372887873030
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 ANDA212707 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03)
source: ndc

Packages (1)

72887-873-03 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03)

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": "2d7ed9b4-3cba-fb22-e063-6294a90af27a", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372887873030"], "unii": ["125OD7737X"], "rxcui": ["2611794"], "spl_set_id": ["1dd56e3d-7ca7-1443-e063-6294a90a13c5"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["FH2 PHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03)", "package_ndc": "72887-873-03", "marketing_start_date": "20240830"}], "brand_name": "methocarbamol", "product_id": "72887-873_2d7ed9b4-3cba-fb22-e063-6294a90af27a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72887-873", "generic_name": "methocarbamol", "labeler_name": "FH2 PHARMA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "1000 mg/1"}], "application_number": "ANDA212707", "marketing_category": "ANDA", "marketing_start_date": "20240830", "listing_expiration_date": "20261231"}