baclofen

Generic: baclofen

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

baclofen 20 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-344
Product ID 29300-344_513de439-4155-4a5d-a25c-bced499e293a
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 29300344
Hyphenated Format 29300-344

Supplemental Identifiers

RxCUI
197391 197392 430902
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 ANDA212067 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (29300-344-01)
  • 500 TABLET in 1 BOTTLE (29300-344-05)
  • 1000 TABLET in 1 BOTTLE (29300-344-10)
  • 90 TABLET in 1 BOTTLE (29300-344-19)
source: ndc

Packages (4)

29300-344-01 100 TABLET in 1 BOTTLE (29300-344-01) 29300-344-05 500 TABLET in 1 BOTTLE (29300-344-05) 29300-344-10 1000 TABLET in 1 BOTTLE (29300-344-10) 29300-344-19 90 TABLET in 1 BOTTLE (29300-344-19)

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": "513de439-4155-4a5d-a25c-bced499e293a", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197391", "197392", "430902"], "spl_set_id": ["b9199878-3fb4-46dc-adbb-b3d9dc3852d4"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (29300-344-01)", "package_ndc": "29300-344-01", "marketing_start_date": "20200709"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (29300-344-05)", "package_ndc": "29300-344-05", "marketing_start_date": "20200709"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (29300-344-10)", "package_ndc": "29300-344-10", "marketing_start_date": "20200709"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (29300-344-19)", "package_ndc": "29300-344-19", "marketing_start_date": "20220825"}], "brand_name": "Baclofen", "product_id": "29300-344_513de439-4155-4a5d-a25c-bced499e293a", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "29300-344", "generic_name": "Baclofen", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "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"}