Package 70868-901-90
Brand: methocarbamol
Generic: methocarbamolPackage Facts
Identity
Package NDC
70868-901-90
Digits Only
7086890190
Product NDC
70868-901
Description
90 TABLET in 1 BOTTLE (70868-901-90)
Marketing
Marketing Status
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": "241421f2-c6b7-78cc-e063-6394a90ae650", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["a88a6c84-b55a-4b6b-ac01-554079f6e304"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Key Therapeutics"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70868-901-90)", "package_ndc": "70868-901-90", "marketing_start_date": "20191226"}], "brand_name": "Methocarbamol", "product_id": "70868-901_241421f2-c6b7-78cc-e063-6394a90ae650", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70868-901", "generic_name": "methocarbamol", "labeler_name": "Key Therapeutics", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20191226", "listing_expiration_date": "20261231"}