Package 67296-2193-1

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 67296-2193-1
Digits Only 6729621931
Product NDC 67296-2193
Description

15 TABLET, FILM COATED in 1 BOTTLE (67296-2193-1)

Marketing

Marketing Status
Marketed Since 2023-02-09
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": "44f2ab95-31bc-f871-e063-6394a90a59bd", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0359651340011"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["44f2aa92-4619-021e-e063-6394a90a296c"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (67296-2193-1)", "package_ndc": "67296-2193-1", "marketing_start_date": "20230209"}], "brand_name": "Methocarbamol", "product_id": "67296-2193_44f2ab95-31bc-f871-e063-6394a90a59bd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "67296-2193", "generic_name": "Methocarbamol", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA213967", "marketing_category": "ANDA", "marketing_start_date": "20230209", "listing_expiration_date": "20261231"}