Package 50090-4793-0

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 50090-4793-0
Digits Only 5009047930
Product NDC 50090-4793
Description

40 TABLET, FILM COATED in 1 BOTTLE (50090-4793-0)

Marketing

Marketing Status
Marketed Since 2019-12-12
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": "60486686-7f0a-400c-bd57-16fed2248fbd", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["ff572473-90e3-4f3b-a40e-8b97b86d327b"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (50090-4793-0)", "package_ndc": "50090-4793-0", "marketing_start_date": "20191212"}], "brand_name": "Methocarbamol", "product_id": "50090-4793_60486686-7f0a-400c-bd57-16fed2248fbd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-4793", "generic_name": "Methocarbamol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20261231"}