baclofen

Generic: baclofen

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name baclofen
Generic Name baclofen
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

baclofen 10 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-394
Product ID 59651-394_493c1b1f-7ee0-4a54-8e44-b2b015eb3850
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)
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 59651394
Hyphenated Format 59651-394

Supplemental Identifiers

RxCUI
197391 197392
UNII
H789N3FKE8
NUI
N0000000196 N0000000116 N0000175759

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59651-394-01)
  • 500 TABLET in 1 BOTTLE (59651-394-05)
  • 1000 TABLET in 1 BOTTLE (59651-394-99)
source: ndc

Packages (3)

Ingredients (1)

baclofen (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "493c1b1f-7ee0-4a54-8e44-b2b015eb3850", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197391", "197392"], "spl_set_id": ["4679a275-9307-4b0f-a2eb-2d83227ea84d"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-394-01)", "package_ndc": "59651-394-01", "marketing_start_date": "20210713"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (59651-394-05)", "package_ndc": "59651-394-05", "marketing_start_date": "20210713"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59651-394-99)", "package_ndc": "59651-394-99", "marketing_start_date": "20210713"}], "brand_name": "BACLOFEN", "product_id": "59651-394_493c1b1f-7ee0-4a54-8e44-b2b015eb3850", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "59651-394", "generic_name": "BACLOFEN", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BACLOFEN", "active_ingredients": [{"name": "BACLOFEN", "strength": "10 mg/1"}], "application_number": "ANDA214099", "marketing_category": "ANDA", "marketing_start_date": "20210713", "listing_expiration_date": "20261231"}