baclofen
Generic: baclofen
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
baclofen
Generic Name
baclofen
Labeler
asclemed usa, inc.
Dosage Form
TABLET
Routes
Active Ingredients
baclofen 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76420-242
Product ID
76420-242_2bbe83e4-da09-81e7-e063-6394a90a1f8e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214099
Listing Expiration
2026-12-31
Marketing Start
2021-07-13
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420242
Hyphenated Format
76420-242
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
ANDA214099 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (76420-242-12)
- 30 TABLET in 1 BOTTLE (76420-242-30)
- 60 TABLET in 1 BOTTLE (76420-242-60)
- 90 TABLET in 1 BOTTLE (76420-242-90)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bbe83e4-da09-81e7-e063-6394a90a1f8e", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197391", "197392"], "spl_set_id": ["687f48da-bc41-4700-9513-77a32fc86c93"], "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": "120 TABLET in 1 BOTTLE (76420-242-12)", "package_ndc": "76420-242-12", "marketing_start_date": "20250115"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-242-30)", "package_ndc": "76420-242-30", "marketing_start_date": "20220725"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-242-60)", "package_ndc": "76420-242-60", "marketing_start_date": "20220725"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-242-90)", "package_ndc": "76420-242-90", "marketing_start_date": "20220725"}], "brand_name": "BACLOFEN", "product_id": "76420-242_2bbe83e4-da09-81e7-e063-6394a90a1f8e", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "76420-242", "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": "ANDA214099", "marketing_category": "ANDA", "marketing_start_date": "20210713", "listing_expiration_date": "20261231"}