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 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-021
Product ID 72789-021_4af30668-89af-69a1-e063-6394a90a38f4
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 72789021
Hyphenated Format 72789-021

Supplemental Identifiers

RxCUI
197943
UPC
0372789021010
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
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-01)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-60)
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-82)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-90)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-93)
  • 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-94)
  • 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-99)
source: ndc

Packages (7)

72789-021-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-01) 72789-021-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-60) 72789-021-82 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-82) 72789-021-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-90) 72789-021-93 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-93) 72789-021-94 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-94) 72789-021-99 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-99)

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": "4af30668-89af-69a1-e063-6394a90a38f4", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789021010"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["943fe701-5d7d-4abe-a529-c5a548e94bc6"], "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": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-01)", "package_ndc": "72789-021-01", "marketing_start_date": "20191024"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-60)", "package_ndc": "72789-021-60", "marketing_start_date": "20230912"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-82)", "package_ndc": "72789-021-82", "marketing_start_date": "20191024"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-90)", "package_ndc": "72789-021-90", "marketing_start_date": "20230912"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-93)", "package_ndc": "72789-021-93", "marketing_start_date": "20191024"}, {"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-94)", "package_ndc": "72789-021-94", "marketing_start_date": "20191024"}, {"sample": false, "description": "240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-99)", "package_ndc": "72789-021-99", "marketing_start_date": "20191024"}], "brand_name": "Methocarbamol", "product_id": "72789-021_4af30668-89af-69a1-e063-6394a90a38f4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-021", "generic_name": "Methocarbamol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20271231"}