Package 76385-124-50

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 76385-124-50
Digits Only 7638512450
Product NDC 76385-124
Product ID 76385-124_1739d3e9-4645-4a0e-bec4-727f8ec63c23
Description

500 TABLET, FILM COATED in 1 BOTTLE (76385-124-50)

Marketing

Marketing Status
Marketed Since 2018-01-15
Brand methocarbamol
Generic methocarbamol
Sample Package No

Linked Drug Pages (1)

Methocarbamol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1739d3e9-4645-4a0e-bec4-727f8ec63c23", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["5777cbb0-b5fd-4b36-ac1d-bc105fe96888"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["UNICHEM PHARMACEUTICALS (USA), INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76385-124-01)", "package_ndc": "76385-124-01", "marketing_start_date": "20180115"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76385-124-50)", "package_ndc": "76385-124-50", "marketing_start_date": "20180115"}], "brand_name": "Methocarbamol", "product_id": "76385-124_1739d3e9-4645-4a0e-bec4-727f8ec63c23", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76385-124", "generic_name": "Methocarbamol", "labeler_name": "UNICHEM PHARMACEUTICALS (USA), INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20271231"}