flumazenil
Generic: flumazenil
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
flumazenil
Generic Name
flumazenil
Labeler
baxter healthcare corporation
Dosage Form
INJECTION
Routes
Active Ingredients
flumazenil .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
36000-149
Product ID
36000-149_f84ae313-68b9-444b-83de-d9f50157dad2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076755
Listing Expiration
2026-12-31
Marketing Start
2017-10-01
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
36000149
Hyphenated Format
36000-149
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
flumazenil (source: ndc)
Generic Name
flumazenil (source: ndc)
Application Number
ANDA076755 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/mL
Packaging
- 10 VIAL, MULTI-DOSE in 1 PACKAGE (36000-149-10) / 10 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f84ae313-68b9-444b-83de-d9f50157dad2", "openfda": {"nui": ["N0000175680"], "unii": ["40P7XK9392"], "rxcui": ["204508"], "spl_set_id": ["8175c1eb-80af-48f1-813c-c8f0e736d894"], "pharm_class_epc": ["Benzodiazepine Antagonist [EPC]"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 PACKAGE (36000-149-10) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "36000-149-10", "marketing_start_date": "20171001"}], "brand_name": "Flumazenil", "product_id": "36000-149_f84ae313-68b9-444b-83de-d9f50157dad2", "dosage_form": "INJECTION", "pharm_class": ["Benzodiazepine Antagonist [EPC]"], "product_ndc": "36000-149", "generic_name": "Flumazenil", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flumazenil", "active_ingredients": [{"name": "FLUMAZENIL", "strength": ".1 mg/mL"}], "application_number": "ANDA076755", "marketing_category": "ANDA", "marketing_start_date": "20171001", "listing_expiration_date": "20261231"}