methocarbamol

Generic: methocarbamol

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8867
Product ID 68788-8867_38d8b457-0c0f-45cb-bf90-965c5a01b198
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213967
Listing Expiration 2026-12-31
Marketing Start 2025-04-23

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 687888867
Hyphenated Format 68788-8867

Supplemental Identifiers

RxCUI
197943
UNII
125OD7737X
NUI
N0000175730 N0000175737

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 ANDA213967 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-8867-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-8867-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-8867-9)
source: ndc

Packages (3)

68788-8867-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-8867-3) 68788-8867-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-8867-6) 68788-8867-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-8867-9)

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": "38d8b457-0c0f-45cb-bf90-965c5a01b198", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["38d8b457-0c0f-45cb-bf90-965c5a01b198"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8867-3)", "package_ndc": "68788-8867-3", "marketing_start_date": "20250423"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8867-6)", "package_ndc": "68788-8867-6", "marketing_start_date": "20250423"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8867-9)", "package_ndc": "68788-8867-9", "marketing_start_date": "20250423"}], "brand_name": "Methocarbamol", "product_id": "68788-8867_38d8b457-0c0f-45cb-bf90-965c5a01b198", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-8867", "generic_name": "Methocarbamol", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA213967", "marketing_category": "ANDA", "marketing_start_date": "20250423", "listing_expiration_date": "20261231"}