methocarbamol

Generic: methocarbamol

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-954
Product ID 82804-954_e4ebe9cf-a274-47c7-b740-4b3d6e9dc52b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040489
Listing Expiration 2027-12-31
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 82804954
Hyphenated Format 82804-954

Supplemental Identifiers

RxCUI
197943 197944
UPC
0382804955305 0382804954308
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
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82804-954-00)
  • 30 TABLET in 1 BOTTLE (82804-954-30)
  • 500 TABLET in 1 BOTTLE (82804-954-55)
  • 60 TABLET in 1 BOTTLE (82804-954-60)
  • 120 TABLET in 1 BOTTLE (82804-954-72)
  • 90 TABLET in 1 BOTTLE (82804-954-90)
source: ndc

Packages (6)

82804-954-00 100 TABLET in 1 BOTTLE (82804-954-00) 82804-954-30 30 TABLET in 1 BOTTLE (82804-954-30) 82804-954-55 500 TABLET in 1 BOTTLE (82804-954-55) 82804-954-60 60 TABLET in 1 BOTTLE (82804-954-60) 82804-954-72 120 TABLET in 1 BOTTLE (82804-954-72) 82804-954-90 90 TABLET in 1 BOTTLE (82804-954-90)

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": "e4ebe9cf-a274-47c7-b740-4b3d6e9dc52b", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0382804955305", "0382804954308"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["e4ebe9cf-a274-47c7-b740-4b3d6e9dc52b"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82804-954-00)", "package_ndc": "82804-954-00", "marketing_start_date": "20260112"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-954-30)", "package_ndc": "82804-954-30", "marketing_start_date": "20260112"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-954-55)", "package_ndc": "82804-954-55", "marketing_start_date": "20260112"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-954-60)", "package_ndc": "82804-954-60", "marketing_start_date": "20260112"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-954-72)", "package_ndc": "82804-954-72", "marketing_start_date": "20260112"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-954-90)", "package_ndc": "82804-954-90", "marketing_start_date": "20260112"}], "brand_name": "Methocarbamol", "product_id": "82804-954_e4ebe9cf-a274-47c7-b740-4b3d6e9dc52b", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "82804-954", "generic_name": "methocarbamol", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20190815", "listing_expiration_date": "20271231"}