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
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7980
Product ID 68788-7980_548ebcd2-1b13-46a2-adc8-da5e40edd0c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040489
Listing Expiration 2026-12-31
Marketing Start 2019-08-15

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 687887980
Hyphenated Format 68788-7980

Supplemental Identifiers

RxCUI
197944
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 ANDA040489 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-7980-3)
  • 60 TABLET in 1 BOTTLE (68788-7980-6)
  • 90 TABLET in 1 BOTTLE (68788-7980-9)
source: ndc

Packages (3)

68788-7980-3 30 TABLET in 1 BOTTLE (68788-7980-3) 68788-7980-6 60 TABLET in 1 BOTTLE (68788-7980-6) 68788-7980-9 90 TABLET in 1 BOTTLE (68788-7980-9)

Ingredients (1)

methocarbamol (750 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": "548ebcd2-1b13-46a2-adc8-da5e40edd0c4", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["4ef1c2c0-31e1-4f85-b645-ff47a057a994"], "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 in 1 BOTTLE (68788-7980-3)", "package_ndc": "68788-7980-3", "marketing_start_date": "20190815"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7980-6)", "package_ndc": "68788-7980-6", "marketing_start_date": "20190815"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7980-9)", "package_ndc": "68788-7980-9", "marketing_start_date": "20190815"}], "brand_name": "Methocarbamol", "product_id": "68788-7980_548ebcd2-1b13-46a2-adc8-da5e40edd0c4", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-7980", "generic_name": "methocarbamol", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20190815", "listing_expiration_date": "20261231"}