Package 76420-359-60

Brand: baclofen

Generic: baclofen
NDC Package

Package Facts

Identity

Package NDC 76420-359-60
Digits Only 7642035960
Product NDC 76420-359
Description

60 TABLET in 1 BOTTLE (76420-359-60)

Marketing

Marketing Status
Marketed Since 2025-05-22
Brand baclofen
Generic baclofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c3b62bc-64f9-f0cb-e063-6394a90a4a92", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197391", "197392", "430902", "2679605"], "spl_set_id": ["35bccefe-8d2e-85b5-e063-6394a90a58ca"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (76420-359-00)", "package_ndc": "76420-359-00", "marketing_start_date": "20250522"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-359-01)", "package_ndc": "76420-359-01", "marketing_start_date": "20250522"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-359-05)", "package_ndc": "76420-359-05", "marketing_start_date": "20250522"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-359-30)", "package_ndc": "76420-359-30", "marketing_start_date": "20250522"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-359-60)", "package_ndc": "76420-359-60", "marketing_start_date": "20250522"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-359-90)", "package_ndc": "76420-359-90", "marketing_start_date": "20250522"}], "brand_name": "BACLOFEN", "product_id": "76420-359_3c3b62bc-64f9-f0cb-e063-6394a90a4a92", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "76420-359", "generic_name": "BACLOFEN", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BACLOFEN", "active_ingredients": [{"name": "BACLOFEN", "strength": "20 mg/1"}], "application_number": "ANDA209102", "marketing_category": "ANDA", "marketing_start_date": "20180401", "listing_expiration_date": "20261231"}