Flumazenil

Product NDC
0641-6032
11-digit product format
006416032
Labeler code
0641
Product ID
0641-6032_d441809f-34f5-4ad8-ad17-9f224aa329ff
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Flumazenil
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
West-ward Pharmaceutical Corp.
Application
ANDA076787
Marketing category
ANDA
Marketing start
2004-10-12
Marketing end
0000-00-00
Substance
FLUMAZENIL
Active strength
0 mg/mL
Pharmacologic classes
Benzodiazepine Antagonist [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0641-6032-102019-11-13C16284748780-197449f38-c9ec-f6ea-e053-dbdaa90aa70317f3ea88-b403-4ee3-840a-640a0b9682b7

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0641-6032-01ML - Milliliter0641-6032168f0c44-881c-4e7d-973e-a74b4d5bd99812013-02-13
0641-6032-10ML - Milliliter0641-6032bb3ecd81-24d2-4780-93a8-07538957236712013-02-13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0641-6032FLUMAZENIL INJECTION [WEST-WARD PHARMACEUTICAL CORP.]1Legacy NDC20120611_17f3ea88-b403-4ee3-840a-640a0b9682b7.zip