FLUTICASONE
- Product NDC
- 55700-680
- 11-digit product format
- 557000680
- Labeler code
- 55700
- Product ID
- 55700-680_ca7c33dc-d237-4f70-a80e-c0ddcc82d011
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluticasone propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078492
- Marketing category
- ANDA
- Marketing start
- 2018-09-07
- Marketing end
- 0000-00-00
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 50 ug/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-680-16 | 55700068016 | 1 BOTTLE, SPRAY in 1 BOX (55700-680-16) > 120 SPRAY, METERED in 1 BOTTLE, SPRAY | 2018-09-07 | 0000-00-00 | No | No | Current |