Flunisolide

Product NDC
64980-510
11-digit product format
649800510
Labeler code
64980
Product ID
64980-510_3f3d300d-a843-4da8-90d1-7a1a4c283c51
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Flunisolide
Dosage form
SPRAY, METERED
Route
NASAL
Labeler
Rising Pharmaceuticals, Inc
Application
ANDA077704
Marketing category
ANDA
Marketing start
2006-08-03
Marketing end
0000-00-00
Substance
FLUNISOLIDE
Active strength
0 mg/mL
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64980-510-252024-03-18C16284748780-19d75b9d0-3e41-f424-e053-dadaa90a57ce3f3d300d-a843-4da8-90d1-7a1a4c283c51
64980-510-252020-01-31C16284748780-19d75b9d0-3e41-f424-e053-dadaa90a57ce3f3d300d-a843-4da8-90d1-7a1a4c283c51

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64980-510-25ML - Milliliter64980-510b179e5cf-38ac-4a20-8dbd-1441119e7d1a12013-07-02