baclofen
Generic: baclofen
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
baclofen
Generic Name
baclofen
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
baclofen 1000 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-680
Product ID
25021-680_81266703-bafa-4e31-a400-32fbfe1a849e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210315
Listing Expiration
2026-12-31
Marketing Start
2021-07-15
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021680
Hyphenated Format
25021-680
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA210315 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 ug/mL
Packaging
- 1 VIAL in 1 CARTON (25021-680-20) / 20 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRATHECAL"], "spl_id": "81266703-bafa-4e31-a400-32fbfe1a849e", "openfda": {"nui": ["N0000000196", "N0000000116", "N0000175759"], "unii": ["H789N3FKE8"], "rxcui": ["1300890"], "spl_set_id": ["d4bfba33-9f4d-4c43-ae6c-bcf67ef8fe51"], "pharm_class_epc": ["gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-680-20) / 20 mL in 1 VIAL", "package_ndc": "25021-680-20", "marketing_start_date": "20210715"}], "brand_name": "Baclofen", "product_id": "25021-680_81266703-bafa-4e31-a400-32fbfe1a849e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["GABA A Agonists [MoA]", "GABA B Agonists [MoA]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "25021-680", "generic_name": "Baclofen", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Baclofen", "active_ingredients": [{"name": "BACLOFEN", "strength": "1000 ug/mL"}], "application_number": "ANDA210315", "marketing_category": "ANDA", "marketing_start_date": "20210715", "listing_expiration_date": "20261231"}