baclofen

Generic: baclofen

Labeler: phoenix rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name baclofen
Generic Name baclofen
Labeler phoenix rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

baclofen 20 mg/1

Manufacturer
PHOENIX RX LLC

Identifiers & Regulatory

Product NDC 85509-1344
Product ID 85509-1344_45c6d07c-9d2b-91c2-e063-6394a90aecfd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212067
Listing Expiration 2026-12-31
Marketing Start 2020-07-09

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 855091344
Hyphenated Format 85509-1344

Supplemental Identifiers

RxCUI
197392
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 ANDA212067 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (85509-1344-3)
  • 60 TABLET in 1 BOTTLE (85509-1344-6)
  • 90 TABLET in 1 BOTTLE (85509-1344-9)
source: ndc

Packages (3)

85509-1344-3 30 TABLET in 1 BOTTLE (85509-1344-3) 85509-1344-6 60 TABLET in 1 BOTTLE (85509-1344-6) 85509-1344-9 90 TABLET in 1 BOTTLE (85509-1344-9)

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": "45c6d07c-9d2b-91c2-e063-6394a90aecfd", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197392"], "spl_set_id": ["45c6d45d-95d5-21b8-e063-6294a90a7955"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (85509-1344-3)", "package_ndc": "85509-1344-3", "marketing_start_date": "20251212"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (85509-1344-6)", "package_ndc": "85509-1344-6", "marketing_start_date": "20251212"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (85509-1344-9)", "package_ndc": "85509-1344-9", "marketing_start_date": "20251212"}], "brand_name": "Baclofen", "product_id": "85509-1344_45c6d07c-9d2b-91c2-e063-6394a90aecfd", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "85509-1344", "generic_name": "Baclofen", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "20 mg/1"}], "application_number": "ANDA212067", "marketing_category": "ANDA", "marketing_start_date": "20200709", "listing_expiration_date": "20261231"}