Package 71205-068-45
Brand: methocarbamol
Generic: methocarbamol tabletsPackage Facts
Identity
Package NDC
71205-068-45
Digits Only
7120506845
Product NDC
71205-068
Description
45 TABLET, COATED in 1 BOTTLE (71205-068-45)
Marketing
Marketing Status
Brand
methocarbamol
Generic
methocarbamol tablets
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0073dfe4-2772-4fc6-a391-504cd2c4a8fb", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0371205068301"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["f6193255-0e83-4510-bc86-30c926ee8fd1"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (71205-068-20)", "package_ndc": "71205-068-20", "marketing_start_date": "20180801"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71205-068-30)", "package_ndc": "71205-068-30", "marketing_start_date": "20180702"}, {"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE (71205-068-40)", "package_ndc": "71205-068-40", "marketing_start_date": "20180702"}, {"sample": false, "description": "45 TABLET, COATED in 1 BOTTLE (71205-068-45)", "package_ndc": "71205-068-45", "marketing_start_date": "20180801"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (71205-068-60)", "package_ndc": "71205-068-60", "marketing_start_date": "20180801"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71205-068-90)", "package_ndc": "71205-068-90", "marketing_start_date": "20180801"}], "brand_name": "Methocarbamol", "product_id": "71205-068_0073dfe4-2772-4fc6-a391-504cd2c4a8fb", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71205-068", "generic_name": "Methocarbamol Tablets", "labeler_name": "Proficient Rx LP", "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": "20180702", "listing_expiration_date": "20261231"}