baclofen

Generic: baclofen

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name baclofen
Generic Name baclofen
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

baclofen 10 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0172-4096
Product ID 0172-4096_ba227be6-e946-423c-a9a6-e0626d889ea7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072234
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 01724096
Hyphenated Format 0172-4096

Supplemental Identifiers

RxCUI
197391 197392
UPC
0301724096608 0301724097605
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 ANDA072234 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0172-4096-60)
  • 1000 TABLET in 1 BOTTLE (0172-4096-80)
source: ndc

Packages (2)

Ingredients (1)

baclofen (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ba227be6-e946-423c-a9a6-e0626d889ea7", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "upc": ["0301724096608", "0301724097605"], "unii": ["H789N3FKE8"], "rxcui": ["197391", "197392"], "spl_set_id": ["5648c772-50cb-4961-996e-e68a8eb699ea"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0172-4096-60)", "package_ndc": "0172-4096-60", "marketing_start_date": "19880721"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0172-4096-80)", "package_ndc": "0172-4096-80", "marketing_start_date": "19880721"}], "brand_name": "Baclofen", "product_id": "0172-4096_ba227be6-e946-423c-a9a6-e0626d889ea7", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "0172-4096", "generic_name": "Baclofen", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "10 mg/1"}], "application_number": "ANDA072234", "marketing_category": "ANDA", "marketing_start_date": "19880721", "listing_expiration_date": "20261231"}