Package 82804-242-30

Brand: baclofen

Generic: baclofen
NDC Package

Package Facts

Identity

Package NDC 82804-242-30
Digits Only 8280424230
Product NDC 82804-242
Description

30 TABLET in 1 BOTTLE (82804-242-30)

Marketing

Marketing Status
Marketed Since 2025-11-07
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": "417434af-df40-42f0-9a34-9127ddafd503", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "upc": ["0382804242900"], "unii": ["H789N3FKE8"], "rxcui": ["197391"], "spl_set_id": ["0680301a-1649-46c4-b74e-ab03967945d0"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (82804-242-20)", "package_ndc": "82804-242-20", "marketing_start_date": "20251229"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-242-30)", "package_ndc": "82804-242-30", "marketing_start_date": "20251107"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-242-60)", "package_ndc": "82804-242-60", "marketing_start_date": "20251028"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-242-72)", "package_ndc": "82804-242-72", "marketing_start_date": "20251009"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (82804-242-78)", "package_ndc": "82804-242-78", "marketing_start_date": "20251028"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-242-90)", "package_ndc": "82804-242-90", "marketing_start_date": "20250905"}], "brand_name": "BACLOFEN", "product_id": "82804-242_417434af-df40-42f0-9a34-9127ddafd503", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "82804-242", "generic_name": "BACLOFEN", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BACLOFEN", "active_ingredients": [{"name": "BACLOFEN", "strength": "10 mg/1"}], "application_number": "ANDA209102", "marketing_category": "ANDA", "marketing_start_date": "20180401", "listing_expiration_date": "20271231"}