Package 76420-040-30

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 76420-040-30
Digits Only 7642004030
Product NDC 76420-040
Description

30 TABLET, FILM COATED in 1 BOTTLE (76420-040-30)

Marketing

Marketing Status
Marketed Since 2020-01-23
Brand methocarbamol
Generic methocarbamol
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ead159e0-3579-29c9-e053-2a95a90a77ad", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["c40d5c1d-9bd8-44aa-85a4-e1a34e1d3673"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-040-30)", "package_ndc": "76420-040-30", "marketing_start_date": "20200123"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-040-60)", "package_ndc": "76420-040-60", "marketing_start_date": "20200123"}], "brand_name": "Methocarbamol", "product_id": "76420-040_ead159e0-3579-29c9-e053-2a95a90a77ad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-040", "generic_name": "Methocarbamol", "labeler_name": "Asclemed 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": "20261231"}