methocarbamol

Generic: methocarbamol

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

methocarbamol 750 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-041
Product ID 72789-041_4af347a6-c3c7-7d45-e063-6294a90a1132
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208507
Listing Expiration 2027-12-31
Marketing Start 2018-01-15

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 72789041
Hyphenated Format 72789-041

Supplemental Identifiers

RxCUI
197944
UPC
0372789041308
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 ANDA208507 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30)
  • 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)
source: ndc

Packages (4)

72789-041-20 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20) 72789-041-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30) 72789-041-40 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40) 72789-041-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)

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": "4af347a6-c3c7-7d45-e063-6294a90a1132", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789041308"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["440bf1ba-a704-4c35-bece-0a0987fc0c11"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20)", "package_ndc": "72789-041-20", "marketing_start_date": "20200213"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30)", "package_ndc": "72789-041-30", "marketing_start_date": "20200116"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40)", "package_ndc": "72789-041-40", "marketing_start_date": "20200106"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)", "package_ndc": "72789-041-60", "marketing_start_date": "20191219"}], "brand_name": "Methocarbamol", "product_id": "72789-041_4af347a6-c3c7-7d45-e063-6294a90a1132", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-041", "generic_name": "Methocarbamol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20271231"}