flumazenil
Generic: flumazenil
Labeler: hf acquisition co. llc, dba healthfirstDrug Facts
Product Profile
Brand Name
flumazenil
Generic Name
flumazenil
Labeler
hf acquisition co. llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
flumazenil .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1254
Product ID
51662-1254_100d725a-9db5-5dd8-e063-6294a90a0797
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078527
Listing Expiration
2026-12-31
Marketing Start
2018-09-01
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621254
Hyphenated Format
51662-1254
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
flumazenil (source: ndc)
Generic Name
flumazenil (source: ndc)
Application Number
ANDA078527 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/mL
Packaging
- 5 mL in 1 VIAL, MULTI-DOSE (51662-1254-1)
- 10 POUCH in 1 CASE (51662-1254-3) / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1254-2) / 5 mL in 1 VIAL, MULTI-DOSE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "100d725a-9db5-5dd8-e063-6294a90a0797", "openfda": {"nui": ["N0000175680"], "unii": ["40P7XK9392"], "rxcui": ["204508"], "spl_set_id": ["74d007e9-9604-0941-e053-2a91aa0a29c4"], "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 (51662-1254-1)", "package_ndc": "51662-1254-1", "marketing_start_date": "20180901"}, {"sample": false, "description": "10 POUCH in 1 CASE (51662-1254-3) / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1254-2) / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "51662-1254-3", "marketing_start_date": "20180901"}], "brand_name": "FLUMAZENIL", "product_id": "51662-1254_100d725a-9db5-5dd8-e063-6294a90a0797", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine Antagonist [EPC]"], "product_ndc": "51662-1254", "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": "ANDA078527", "marketing_category": "ANDA", "marketing_start_date": "20180901", "listing_expiration_date": "20261231"}