Package 55111-650-01

Brand: metaxalone

Generic: metaxalone
NDC Package

Package Facts

Identity

Package NDC 55111-650-01
Digits Only 5511165001
Product NDC 55111-650
Description

100 TABLET in 1 BOTTLE (55111-650-01)

Marketing

Marketing Status
Marketed Since 2017-08-31
Brand metaxalone
Generic metaxalone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c27dda6-06ef-c6ae-e063-6294a90a8ff2", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["1NMA9J598Y"], "rxcui": ["351254"], "spl_set_id": ["02eb5938-cd59-4a81-853d-a4148d813a94"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Dr. Reddys Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-650-01)", "package_ndc": "55111-650-01", "marketing_start_date": "20170831"}], "brand_name": "Metaxalone", "product_id": "55111-650_2c27dda6-06ef-c6ae-e063-6294a90a8ff2", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "55111-650", "generic_name": "Metaxalone", "labeler_name": "Dr. Reddys Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metaxalone", "active_ingredients": [{"name": "METAXALONE", "strength": "800 mg/1"}], "application_number": "ANDA207466", "marketing_category": "ANDA", "marketing_start_date": "20170831", "listing_expiration_date": "20261231"}