FLUTICASONE
- Product NDC
- 71205-443
- 11-digit product format
- 712050443
- Labeler code
- 71205
- Product ID
- 71205-443_ebef6621-2fa3-49b4-b30a-7e5313918ca9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluticasone propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078492
- Marketing category
- ANDA
- Marketing start
- 2012-01-09
- Marketing end
- 0000-00-00
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 50 ug/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-443 | FLUTICASONE (FLUTICASONE PROPIONATE) SPRAY, METERED [PROFICIENT RX LP] | 3 | Legacy NDC | 20241018_40d1d0f5-0657-465e-9fe7-4afe9e0f7fbe.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-443-16 | 71205044316 | 1 BOTTLE, SPRAY in 1 BOX (71205-443-16) > 120 SPRAY, METERED in 1 BOTTLE, SPRAY | 2020-10-29 | 0000-00-00 | No | No | Current |