methocarbamol

Generic: methocarbamol

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler somerset therapeutics, llc
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

methocarbamol 100 mg/mL

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-101
Product ID 70069-101_dd175ad9-9f83-4ef1-b745-65e44f5e12c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207522
Listing Expiration 2026-12-31
Marketing Start 2017-07-31

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 70069101
Hyphenated Format 70069-101

Supplemental Identifiers

RxCUI
238175
UPC
0370069101018 0370069101100 0370069101254 0370069101056
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 ANDA207522 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
Packaging
  • 5 VIAL in 1 CARTON (70069-101-05) / 10 mL in 1 VIAL
  • 10 VIAL in 1 CARTON (70069-101-10) / 10 mL in 1 VIAL
  • 25 VIAL in 1 CARTON (70069-101-25) / 10 mL in 1 VIAL
source: ndc

Packages (3)

Ingredients (1)

methocarbamol (100 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "dd175ad9-9f83-4ef1-b745-65e44f5e12c4", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0370069101018", "0370069101100", "0370069101254", "0370069101056"], "unii": ["125OD7737X"], "rxcui": ["238175"], "spl_set_id": ["68dd9c24-4d41-48be-9f54-fceb787bb443"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (70069-101-05)  / 10 mL in 1 VIAL", "package_ndc": "70069-101-05", "marketing_start_date": "20170731"}, {"sample": false, "description": "10 VIAL in 1 CARTON (70069-101-10)  / 10 mL in 1 VIAL", "package_ndc": "70069-101-10", "marketing_start_date": "20170731"}, {"sample": false, "description": "25 VIAL in 1 CARTON (70069-101-25)  / 10 mL in 1 VIAL", "package_ndc": "70069-101-25", "marketing_start_date": "20170731"}], "brand_name": "Methocarbamol", "product_id": "70069-101_dd175ad9-9f83-4ef1-b745-65e44f5e12c4", "dosage_form": "INJECTION", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70069-101", "generic_name": "Methocarbamol", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "100 mg/mL"}], "application_number": "ANDA207522", "marketing_category": "ANDA", "marketing_start_date": "20170731", "listing_expiration_date": "20261231"}