Package 71335-2669-3

Brand: baclofen

Generic: baclofen
NDC Package

Package Facts

Identity

Package NDC 71335-2669-3
Digits Only 7133526693
Product NDC 71335-2669
Description

120 TABLET in 1 BOTTLE (71335-2669-3)

Marketing

Marketing Status
Marketed Since 2025-06-26
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": "21d9a176-5277-4fa4-83c5-91ef3743368d", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197392"], "spl_set_id": ["3ac0f0d2-86d8-46d0-88e5-c243734b0814"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2669-1)", "package_ndc": "71335-2669-1", "marketing_start_date": "20250626"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2669-2)", "package_ndc": "71335-2669-2", "marketing_start_date": "20250626"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2669-3)", "package_ndc": "71335-2669-3", "marketing_start_date": "20250626"}], "brand_name": "Baclofen", "product_id": "71335-2669_21d9a176-5277-4fa4-83c5-91ef3743368d", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "71335-2669", "generic_name": "Baclofen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "20 mg/1"}], "application_number": "ANDA212378", "marketing_category": "ANDA", "marketing_start_date": "20240615", "listing_expiration_date": "20261231"}