Package 87063-040-20

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 87063-040-20
Digits Only 8706304020
Product NDC 87063-040
Description

20 TABLET, FILM COATED in 1 BOTTLE (87063-040-20)

Marketing

Marketing Status
Marketed Since 2025-11-24
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": "445114b8-5b56-c48d-e063-6294a90a31d1", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["7f297ac6-a580-4539-a770-fe5d15c2b922"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (87063-040-01)", "package_ndc": "87063-040-01", "marketing_start_date": "20251124"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (87063-040-10)", "package_ndc": "87063-040-10", "marketing_start_date": "20251124"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (87063-040-20)", "package_ndc": "87063-040-20", "marketing_start_date": "20251124"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (87063-040-30)", "package_ndc": "87063-040-30", "marketing_start_date": "20251124"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (87063-040-60)", "package_ndc": "87063-040-60", "marketing_start_date": "20251124"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (87063-040-90)", "package_ndc": "87063-040-90", "marketing_start_date": "20251124"}], "brand_name": "Methocarbamol", "product_id": "87063-040_445114b8-5b56-c48d-e063-6294a90a31d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "87063-040", "generic_name": "Methocarbamol", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA213967", "marketing_category": "ANDA", "marketing_start_date": "20230209", "listing_expiration_date": "20261231"}