methocarbamol
Generic: methocarbamol
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
methocarbamol
Generic Name
methocarbamol
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
methocarbamol 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
66267-803
Product ID
66267-803_1fa77075-a199-971d-e063-6294a90a255d
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
66267803
Hyphenated Format
66267-803
Supplemental Identifiers
RxCUI
UPC
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
- 6 TABLET in 1 BOTTLE (66267-803-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1fa77075-a199-971d-e063-6294a90a255d", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0366267803069"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["9d6024b2-ee1a-3a79-e053-2a95a90a1bf4"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (66267-803-06)", "package_ndc": "66267-803-06", "marketing_start_date": "20200130"}], "brand_name": "Methocarbamol", "product_id": "66267-803_1fa77075-a199-971d-e063-6294a90a255d", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "66267-803", "generic_name": "Methocarbamol", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}