Package 70868-910-10
Brand: methocarbamol
Generic: methocarbamolPackage Facts
Identity
Package NDC
70868-910-10
Digits Only
7086891010
Product NDC
70868-910
Description
100 TABLET in 1 BOTTLE (70868-910-10)
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": "24143189-700c-75f8-e063-6394a90ac5ce", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["cf931001-95bd-4900-98d5-f5ef54b49d99"], "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": "100 TABLET in 1 BOTTLE (70868-910-10)", "package_ndc": "70868-910-10", "marketing_start_date": "20210101"}], "brand_name": "Methocarbamol", "product_id": "70868-910_24143189-700c-75f8-e063-6394a90ac5ce", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70868-910", "generic_name": "methocarbamol", "labeler_name": "Key Therapeutics", "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": "20210101", "listing_expiration_date": "20261231"}