methocarb 500-ezs

Generic: methocarbamol

Labeler: puretek corporation
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name methocarb 500-ezs
Generic Name methocarbamol
Labeler puretek corporation
Dosage Form KIT
Manufacturer
PureTek Corporation

Identifiers & Regulatory

Product NDC 59088-724
Product ID 59088-724_b3ca019e-98e0-1007-e053-2a95a90a1690
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2018-10-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59088724
Hyphenated Format 59088-724

Supplemental Identifiers

RxCUI
197943
UPC
0731477272217

Packaging Origin

Original Packager
true

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 methocarb 500-ezs (source: ndc)
Generic Name methocarbamol (source: ndc)

Resolved Composition

Strengths
  • 500 mg
  • 750 mg
source: label
Packaging
  • 1 KIT in 1 KIT (59088-724-00) * 100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10)
source: ndc

Packages (1)

59088-724-00 1 KIT in 1 KIT (59088-724-00) * 100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Methocarb 500-EZS ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "b3ca019e-98e0-1007-e053-2a95a90a1690", "openfda": {"upc": ["0731477272217"], "rxcui": ["197943"], "spl_set_id": ["383ce408-1085-43e7-944e-957ff2a9d553"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (59088-724-00)  *  100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10)", "package_ndc": "59088-724-00", "marketing_start_date": "20181023"}], "brand_name": "Methocarb 500-EZS", "product_id": "59088-724_b3ca019e-98e0-1007-e053-2a95a90a1690", "dosage_form": "KIT", "product_ndc": "59088-724", "generic_name": "Methocarbamol", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarb 500-EZS", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20181023", "listing_expiration_date": "20261231"}