methocarbamol

Generic: methocarbamol tablets

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol tablets
Labeler northwind health company, llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-195
Product ID 51655-195_48c437b6-0095-daf8-e063-6394a90a6a1c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209312
Listing Expiration 2027-12-31
Marketing Start 2022-11-16

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 51655195
Hyphenated Format 51655-195

Supplemental Identifiers

RxCUI
197943
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 tablets (source: ndc)
Application Number ANDA209312 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 40 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-51)
  • 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-52)
  • 14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-84)
source: ndc

Packages (3)

51655-195-51 40 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-51) 51655-195-52 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-52) 51655-195-84 14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-84)

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": "48c437b6-0095-daf8-e063-6394a90a6a1c", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["f2b4ed95-0469-393a-e053-2a95a90a98ed"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-51)", "package_ndc": "51655-195-51", "marketing_start_date": "20221216"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-52)", "package_ndc": "51655-195-52", "marketing_start_date": "20221216"}, {"sample": false, "description": "14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-84)", "package_ndc": "51655-195-84", "marketing_start_date": "20221116"}], "brand_name": "Methocarbamol", "product_id": "51655-195_48c437b6-0095-daf8-e063-6394a90a6a1c", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "51655-195", "generic_name": "Methocarbamol Tablets", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_start_date": "20221116", "listing_expiration_date": "20271231"}