Package 70518-3117-2

Brand: Methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 70518-3117-2
Digits Only 7051831172
Product NDC 70518-3117
Description

15 TABLET in 1 BOTTLE, PLASTIC (70518-3117-2)

Marketing

Marketing Status
Marketed Since 2024-09-29
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": "3e726802-1da2-7a7a-e063-6294a90a39cd", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["d34fd746-3f43-429a-987f-72ad7228a8a2"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (70518-3117-2)", "package_ndc": "70518-3117-2", "marketing_start_date": "20240929"}], "brand_name": "Methocarbamol", "product_id": "70518-3117_3e726802-1da2-7a7a-e063-6294a90a39cd", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-3117", "generic_name": "methocarbamol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20210610", "listing_expiration_date": "20261231"}