baclofen
Generic: baclofen
Labeler: advanced rx pharmacy of tennessee, llcDrug Facts
Product Profile
Brand Name
baclofen
Generic Name
baclofen
Labeler
advanced rx pharmacy of tennessee, llc
Dosage Form
TABLET
Routes
Active Ingredients
baclofen 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
80425-0156
Product ID
80425-0156_2a99a7c1-c4c2-2b01-e063-6294a90aa3b8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212378
Listing Expiration
2026-12-31
Marketing Start
2020-10-09
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
804250156
Hyphenated Format
80425-0156
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
baclofen (source: ndc)
Generic Name
baclofen (source: ndc)
Application Number
ANDA212378 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (80425-0156-1)
- 60 TABLET in 1 BOTTLE (80425-0156-2)
- 90 TABLET in 1 BOTTLE (80425-0156-3)
- 120 TABLET in 1 BOTTLE (80425-0156-4)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a99a7c1-c4c2-2b01-e063-6294a90aa3b8", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197391"], "spl_set_id": ["c85a1884-f46f-5cd4-e053-2a95a90a3e27"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0156-1)", "package_ndc": "80425-0156-1", "marketing_start_date": "20201009"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0156-2)", "package_ndc": "80425-0156-2", "marketing_start_date": "20201009"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0156-3)", "package_ndc": "80425-0156-3", "marketing_start_date": "20201009"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (80425-0156-4)", "package_ndc": "80425-0156-4", "marketing_start_date": "20230518"}], "brand_name": "Baclofen", "product_id": "80425-0156_2a99a7c1-c4c2-2b01-e063-6294a90aa3b8", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "80425-0156", "generic_name": "Baclofen", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "10 mg/1"}], "application_number": "ANDA212378", "marketing_category": "ANDA", "marketing_start_date": "20201009", "listing_expiration_date": "20261231"}