methocarbamol
Generic: methocarbamol
Labeler: somerset therapeutics, llcDrug Facts
Product Profile
Brand Name
methocarbamol
Generic Name
methocarbamol
Labeler
somerset therapeutics, llc
Dosage Form
INJECTION
Routes
Active Ingredients
methocarbamol 100 mg/mL
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70069101
Hyphenated Format
70069-101
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
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
Packages (3)
Ingredients (1)
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"}