Package 61919-832-90

Brand: metaxalone

Generic: metaxalone
NDC Package

Package Facts

Identity

Package NDC 61919-832-90
Digits Only 6191983290
Product NDC 61919-832
Product ID 61919-832_47e15fc2-987b-4fa9-e063-6294a90adf51
Description

90 TABLET in 1 BOTTLE (61919-832-90)

Marketing

Marketing Status
Marketed Since 2019-05-03
Brand metaxalone
Generic metaxalone
Sample Package No

Linked Drug Pages (1)

METAXALONE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e15fc2-987b-4fa9-e063-6294a90adf51", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["1NMA9J598Y"], "rxcui": ["351254"], "spl_set_id": ["49250bbf-fbfe-07cd-e054-00144ff88e88"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (61919-832-90)", "package_ndc": "61919-832-90", "marketing_start_date": "20190503"}], "brand_name": "METAXALONE", "product_id": "61919-832_47e15fc2-987b-4fa9-e063-6294a90adf51", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "61919-832", "generic_name": "METAXALONE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METAXALONE", "active_ingredients": [{"name": "METAXALONE", "strength": "800 mg/1"}], "application_number": "ANDA204770", "marketing_category": "ANDA", "marketing_start_date": "20190503", "listing_expiration_date": "20271231"}