Package 72887-873-03

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 72887-873-03
Digits Only 7288787303
Product NDC 72887-873
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03)

Marketing

Marketing Status
Marketed Since 2024-08-30
Brand methocarbamol
Generic methocarbamol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d7ed9b4-3cba-fb22-e063-6294a90af27a", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372887873030"], "unii": ["125OD7737X"], "rxcui": ["2611794"], "spl_set_id": ["1dd56e3d-7ca7-1443-e063-6294a90a13c5"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["FH2 PHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03)", "package_ndc": "72887-873-03", "marketing_start_date": "20240830"}], "brand_name": "methocarbamol", "product_id": "72887-873_2d7ed9b4-3cba-fb22-e063-6294a90af27a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72887-873", "generic_name": "methocarbamol", "labeler_name": "FH2 PHARMA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "1000 mg/1"}], "application_number": "ANDA212707", "marketing_category": "ANDA", "marketing_start_date": "20240830", "listing_expiration_date": "20261231"}