baclofen
Generic: baclofen
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
baclofen
Generic Name
baclofen
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
baclofen 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1079
Product ID
72162-1079_5de12657-b943-4215-8979-d2a285fcd7ec
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078220
Listing Expiration
2026-12-31
Marketing Start
2007-07-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621079
Hyphenated Format
72162-1079
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA078220 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1079-0)
- 100 TABLET in 1 BOTTLE, PLASTIC (72162-1079-1)
- 140 TABLET in 1 BOTTLE, PLASTIC (72162-1079-8)
- 90 TABLET in 1 BOTTLE, PLASTIC (72162-1079-9)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5de12657-b943-4215-8979-d2a285fcd7ec", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197391"], "spl_set_id": ["fc4b99b3-f59f-4e1f-9a8c-123a0c2fbd9f"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72162-1079-0)", "package_ndc": "72162-1079-0", "marketing_start_date": "20230508"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1079-1)", "package_ndc": "72162-1079-1", "marketing_start_date": "20230508"}, {"sample": false, "description": "140 TABLET in 1 BOTTLE, PLASTIC (72162-1079-8)", "package_ndc": "72162-1079-8", "marketing_start_date": "20230508"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72162-1079-9)", "package_ndc": "72162-1079-9", "marketing_start_date": "20230508"}], "brand_name": "Baclofen", "product_id": "72162-1079_5de12657-b943-4215-8979-d2a285fcd7ec", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "72162-1079", "generic_name": "baclofen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "10 mg/1"}], "application_number": "ANDA078220", "marketing_category": "ANDA", "marketing_start_date": "20070701", "listing_expiration_date": "20261231"}