baclofen
Generic: baclofen
Labeler: endo usa, inc.Drug Facts
Product Profile
Brand Name
baclofen
Generic Name
baclofen
Labeler
endo usa, inc.
Dosage Form
TABLET
Routes
Active Ingredients
baclofen 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0603-2406
Product ID
0603-2406_3c181e4e-fead-4e63-8b01-b91bc9099225
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077068
Listing Expiration
2026-12-31
Marketing Start
2005-08-30
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06032406
Hyphenated Format
0603-2406
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
ANDA077068 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (0603-2406-21)
- 500 TABLET in 1 BOTTLE, PLASTIC (0603-2406-28)
- 1000 TABLET in 1 BOTTLE, PLASTIC (0603-2406-32)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c181e4e-fead-4e63-8b01-b91bc9099225", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "upc": ["0306032407214", "0306032406217"], "unii": ["H789N3FKE8"], "rxcui": ["197391", "197392"], "spl_set_id": ["c17527be-661d-42f5-b6f6-56a681ba7870"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0603-2406-21)", "package_ndc": "0603-2406-21", "marketing_start_date": "20050830"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (0603-2406-28)", "package_ndc": "0603-2406-28", "marketing_start_date": "20050830"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0603-2406-32)", "package_ndc": "0603-2406-32", "marketing_start_date": "20050830"}], "brand_name": "Baclofen", "product_id": "0603-2406_3c181e4e-fead-4e63-8b01-b91bc9099225", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "0603-2406", "generic_name": "Baclofen", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "10 mg/1"}], "application_number": "ANDA077068", "marketing_category": "ANDA", "marketing_start_date": "20050830", "listing_expiration_date": "20261231"}