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 72789-012
Product ID 72789-012_4af2fbb0-4343-0414-e063-6294a90aa54c
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 72789012
Hyphenated Format 72789-012

Supplemental Identifiers

RxCUI
197943
UPC
0372789012308
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
  • 18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-18)
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-20)
  • 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-24)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-30)
  • 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40)
source: ndc

Packages (5)

Ingredients (1)

methocarbamol (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4af2fbb0-4343-0414-e063-6294a90aa54c", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789012308"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["288a3bcd-a2c8-4a9b-9602-59c0493b4a8d"], "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": "18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-18)", "package_ndc": "72789-012-18", "marketing_start_date": "20191219"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-20)", "package_ndc": "72789-012-20", "marketing_start_date": "20190920"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-24)", "package_ndc": "72789-012-24", "marketing_start_date": "20210505"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-30)", "package_ndc": "72789-012-30", "marketing_start_date": "20210810"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40)", "package_ndc": "72789-012-40", "marketing_start_date": "20200616"}], "brand_name": "Methocarbamol", "product_id": "72789-012_4af2fbb0-4343-0414-e063-6294a90aa54c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-012", "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"}