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 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0103
Product ID
71335-0103_60ded7d2-5758-4bcb-9aec-928a434f3efc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077241
Listing Expiration
2026-12-31
Marketing Start
2005-12-20
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350103
Hyphenated Format
71335-0103
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
ANDA077241 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (71335-0103-0)
- 90 TABLET in 1 BOTTLE (71335-0103-1)
- 20 TABLET in 1 BOTTLE (71335-0103-2)
- 60 TABLET in 1 BOTTLE (71335-0103-3)
- 45 TABLET in 1 BOTTLE (71335-0103-4)
- 112 TABLET in 1 BOTTLE (71335-0103-5)
- 30 TABLET in 1 BOTTLE (71335-0103-6)
- 56 TABLET in 1 BOTTLE (71335-0103-7)
- 15 TABLET in 1 BOTTLE (71335-0103-8)
- 84 TABLET in 1 BOTTLE (71335-0103-9)
Packages (10)
71335-0103-0
120 TABLET in 1 BOTTLE (71335-0103-0)
71335-0103-1
90 TABLET in 1 BOTTLE (71335-0103-1)
71335-0103-2
20 TABLET in 1 BOTTLE (71335-0103-2)
71335-0103-3
60 TABLET in 1 BOTTLE (71335-0103-3)
71335-0103-4
45 TABLET in 1 BOTTLE (71335-0103-4)
71335-0103-5
112 TABLET in 1 BOTTLE (71335-0103-5)
71335-0103-6
30 TABLET in 1 BOTTLE (71335-0103-6)
71335-0103-7
56 TABLET in 1 BOTTLE (71335-0103-7)
71335-0103-8
15 TABLET in 1 BOTTLE (71335-0103-8)
71335-0103-9
84 TABLET in 1 BOTTLE (71335-0103-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "60ded7d2-5758-4bcb-9aec-928a434f3efc", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["197392"], "spl_set_id": ["58816b46-28a5-48e2-b89d-98df65939386"], "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": "120 TABLET in 1 BOTTLE (71335-0103-0)", "package_ndc": "71335-0103-0", "marketing_start_date": "20180306"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0103-1)", "package_ndc": "71335-0103-1", "marketing_start_date": "20180215"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-0103-2)", "package_ndc": "71335-0103-2", "marketing_start_date": "20211227"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0103-3)", "package_ndc": "71335-0103-3", "marketing_start_date": "20180212"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-0103-4)", "package_ndc": "71335-0103-4", "marketing_start_date": "20211227"}, {"sample": false, "description": "112 TABLET in 1 BOTTLE (71335-0103-5)", "package_ndc": "71335-0103-5", "marketing_start_date": "20211227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0103-6)", "package_ndc": "71335-0103-6", "marketing_start_date": "20180226"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-0103-7)", "package_ndc": "71335-0103-7", "marketing_start_date": "20211227"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-0103-8)", "package_ndc": "71335-0103-8", "marketing_start_date": "20211227"}, {"sample": false, "description": "84 TABLET in 1 BOTTLE (71335-0103-9)", "package_ndc": "71335-0103-9", "marketing_start_date": "20211227"}], "brand_name": "Baclofen", "product_id": "71335-0103_60ded7d2-5758-4bcb-9aec-928a434f3efc", "dosage_form": "TABLET", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "71335-0103", "generic_name": "baclofen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "20 mg/1"}], "application_number": "ANDA077241", "marketing_category": "ANDA", "marketing_start_date": "20051220", "listing_expiration_date": "20261231"}