baclofen
Generic: baclofen
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
baclofen
Generic Name
baclofen
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
baclofen 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-865
Product ID
43063-865_415c3642-f324-746e-e063-6294a90a7ae0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077241
Listing Expiration
2026-12-31
Marketing Start
2005-12-20
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063865
Hyphenated Format
43063-865
Supplemental Identifiers
RxCUI
UPC
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
ANDA077241 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-865-30)
- 60 TABLET in 1 BOTTLE, PLASTIC (43063-865-60)
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-865-90)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415c3642-f324-746e-e063-6294a90a7ae0", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "upc": ["0343063865309", "0343063864906"], "unii": ["H789N3FKE8"], "rxcui": ["197391", "197392"], "spl_set_id": ["cfcf519f-5d15-431d-89c8-961a0c38ba60"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-865-30)", "package_ndc": "43063-865-30", "marketing_start_date": "20180626"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-865-60)", "package_ndc": "43063-865-60", "marketing_start_date": "20180626"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-865-90)", "package_ndc": "43063-865-90", "marketing_start_date": "20180626"}], "brand_name": "Baclofen", "product_id": "43063-865_415c3642-f324-746e-e063-6294a90a7ae0", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "43063-865", "generic_name": "baclofen", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "20 mg/1"}], "application_number": "ANDA077241", "marketing_category": "ANDA", "marketing_start_date": "20051220", "listing_expiration_date": "20261231"}