baclofen

Generic: baclofen

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

Drug Facts

Product Profile

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

baclofen 10 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3700
Product ID 68071-3700_2a0a31f5-29a6-7400-e063-6294a90ab12d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214374
Listing Expiration 2026-12-31
Marketing Start 2024-03-01

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 680713700
Hyphenated Format 68071-3700

Supplemental Identifiers

RxCUI
197391
UPC
0368071370096
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 ANDA214374 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3700-3)
  • 60 TABLET in 1 BOTTLE (68071-3700-6)
  • 90 TABLET in 1 BOTTLE (68071-3700-9)
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": "2a0a31f5-29a6-7400-e063-6294a90ab12d", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "upc": ["0368071370096"], "unii": ["H789N3FKE8"], "rxcui": ["197391"], "spl_set_id": ["2517f71f-f452-1f56-e063-6394a90a6ef1"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3700-3)", "package_ndc": "68071-3700-3", "marketing_start_date": "20241022"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3700-6)", "package_ndc": "68071-3700-6", "marketing_start_date": "20241029"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3700-9)", "package_ndc": "68071-3700-9", "marketing_start_date": "20241022"}], "brand_name": "BACLOFEN", "product_id": "68071-3700_2a0a31f5-29a6-7400-e063-6294a90ab12d", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "68071-3700", "generic_name": "BACLOFEN", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BACLOFEN", "active_ingredients": [{"name": "BACLOFEN", "strength": "10 mg/1"}], "application_number": "ANDA214374", "marketing_category": "ANDA", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}