Package 70518-4501-0
Brand: methocarbamol
Generic: methocarbamol tabletsPackage Facts
Identity
Package NDC
70518-4501-0
Digits Only
7051845010
Product NDC
70518-4501
Description
40 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4501-0)
Marketing
Marketing Status
Brand
methocarbamol
Generic
methocarbamol tablets
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "410c526a-4b20-423b-e063-6294a90ac9fe", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["3e4c88fe-bc3d-463f-973c-e52062e4d4ba"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4501-0)", "package_ndc": "70518-4501-0", "marketing_start_date": "20251013"}], "brand_name": "Methocarbamol", "product_id": "70518-4501_410c526a-4b20-423b-e063-6294a90ac9fe", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-4501", "generic_name": "Methocarbamol Tablets", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_start_date": "20251013", "listing_expiration_date": "20261231"}