Package 72789-110-40

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 72789-110-40
Digits Only 7278911040
Product NDC 72789-110
Description

40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-110-40)

Marketing

Marketing Status
Marketed Since 2020-09-08
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": "4af678cf-57cd-5095-e063-6394a90a04ce", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789110400"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["12c8da39-3a0e-4303-9655-29dd83507837"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-110-40)", "package_ndc": "72789-110-40", "marketing_start_date": "20200908"}], "brand_name": "Methocarbamol", "product_id": "72789-110_4af678cf-57cd-5095-e063-6394a90a04ce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-110", "generic_name": "Methocarbamol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20271231"}