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#