methocarbamol
Generic: methocarbamol
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
methocarbamol
Generic Name
methocarbamol
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
methocarbamol 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-1783
Product ID
50090-1783_704e637c-f62c-42a3-a604-c4d34e6589e4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090200
Listing Expiration
2026-12-31
Marketing Start
2013-03-20
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500901783
Hyphenated Format
50090-1783
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA090200 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-1783-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "704e637c-f62c-42a3-a604-c4d34e6589e4", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["ff55df39-e314-4120-8fab-3757cbe5a872"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-1783-0)", "package_ndc": "50090-1783-0", "marketing_start_date": "20150416"}], "brand_name": "Methocarbamol", "product_id": "50090-1783_704e637c-f62c-42a3-a604-c4d34e6589e4", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-1783", "generic_name": "Methocarbamol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA090200", "marketing_category": "ANDA", "marketing_start_date": "20130320", "listing_expiration_date": "20261231"}