baclofen

Generic: baclofen

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name baclofen
Generic Name baclofen
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

baclofen 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-274
Product ID 63187-274_8ef3522a-3a22-4d52-852d-a18f5a78f482
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072235
Listing Expiration 2026-12-31
Marketing Start 1988-07-21

Pharmacologic Class

Established (EPC)
gamma-aminobutyric acid-ergic agonist [epc]
Mechanism of Action
gaba a agonists [moa] gaba b agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187274
Hyphenated Format 63187-274

Supplemental Identifiers

RxCUI
197392
UPC
0363187274306
UNII
H789N3FKE8
NUI
N0000000196 N0000000116 N0000175759

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 ANDA072235 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63187-274-30)
  • 60 TABLET in 1 BOTTLE (63187-274-60)
  • 90 TABLET in 1 BOTTLE (63187-274-90)
source: ndc

Packages (3)

63187-274-30 30 TABLET in 1 BOTTLE (63187-274-30) 63187-274-60 60 TABLET in 1 BOTTLE (63187-274-60) 63187-274-90 90 TABLET in 1 BOTTLE (63187-274-90)

Ingredients (1)

baclofen (20 mg/1)

Linked Drug Pages (1)

Baclofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8ef3522a-3a22-4d52-852d-a18f5a78f482", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "upc": ["0363187274306"], "unii": ["H789N3FKE8"], "rxcui": ["197392"], "spl_set_id": ["9d5a10cf-9a99-41eb-b4b8-9cf4cfaff6fc"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-274-30)", "package_ndc": "63187-274-30", "marketing_start_date": "20141121"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-274-60)", "package_ndc": "63187-274-60", "marketing_start_date": "20141121"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-274-90)", "package_ndc": "63187-274-90", "marketing_start_date": "20141121"}], "brand_name": "Baclofen", "product_id": "63187-274_8ef3522a-3a22-4d52-852d-a18f5a78f482", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "63187-274", "generic_name": "Baclofen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "20 mg/1"}], "application_number": "ANDA072235", "marketing_category": "ANDA", "marketing_start_date": "19880721", "listing_expiration_date": "20261231"}