Methocarbamol

Generic: methocarbamol

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Methocarbamol
Generic Name methocarbamol
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

METHOCARBAMOL 500 mg/1

Identifiers & Regulatory

Product NDC 70518-3117
Product ID 70518-3117_3e726802-1da2-7a7a-e063-6294a90a39cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040489
Listing Expiration 2026-12-31
Marketing Start 2021-06-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183117
Hyphenated Format 70518-3117

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 ANDA040489 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE, PLASTIC (70518-3117-2)
source: ndc

Packages (1)

70518-3117-2 15 TABLET in 1 BOTTLE, PLASTIC (70518-3117-2)

Ingredients (1)

METHOCARBAMOL (500 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": "3e726802-1da2-7a7a-e063-6294a90a39cd", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["d34fd746-3f43-429a-987f-72ad7228a8a2"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (70518-3117-2)", "package_ndc": "70518-3117-2", "marketing_start_date": "20240929"}], "brand_name": "Methocarbamol", "product_id": "70518-3117_3e726802-1da2-7a7a-e063-6294a90a39cd", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-3117", "generic_name": "methocarbamol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20210610", "listing_expiration_date": "20261231"}