flumazenil

Generic: flumazenil

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flumazenil
Generic Name flumazenil
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

flumazenil .1 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1579
Product ID 51662-1579_c5da455f-3214-ab11-e053-2995a90a54ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076955
Listing Expiration 2026-12-31
Marketing Start 2021-06-28

Pharmacologic Class

Established (EPC)
benzodiazepine antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621579
Hyphenated Format 51662-1579

Supplemental Identifiers

RxCUI
204508
UPC
0363323424053
UNII
40P7XK9392
NUI
N0000175680

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 ANDA076955 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .1 mg/mL
source: ndc
Packaging
  • 5 mL in 1 VIAL, MULTI-DOSE (51662-1579-1)
source: ndc

Packages (1)

Ingredients (1)

flumazenil (.1 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c5da455f-3214-ab11-e053-2995a90a54ee", "openfda": {"nui": ["N0000175680"], "upc": ["0363323424053"], "unii": ["40P7XK9392"], "rxcui": ["204508"], "spl_set_id": ["c5da455f-3213-ab11-e053-2995a90a54ee"], "pharm_class_epc": ["Benzodiazepine Antagonist [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, MULTI-DOSE (51662-1579-1)", "package_ndc": "51662-1579-1", "marketing_start_date": "20210628"}], "brand_name": "FLUMAZENIL", "product_id": "51662-1579_c5da455f-3214-ab11-e053-2995a90a54ee", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine Antagonist [EPC]"], "product_ndc": "51662-1579", "generic_name": "FLUMAZENIL", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUMAZENIL", "active_ingredients": [{"name": "FLUMAZENIL", "strength": ".1 mg/mL"}], "application_number": "ANDA076955", "marketing_category": "ANDA", "marketing_start_date": "20210628", "listing_expiration_date": "20261231"}