Allergy Relief
- Product NDC
- 0536-1373
- 11-digit product format
- 005361373
- Labeler code
- 0536
- Product ID
- 0536-1373_a016ff8f-6a55-4c9e-8891-1cca5fefbb9a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fluticasone propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Rugby Laboratories, Inc.
- Application
- ANDA208024
- Marketing category
- ANDA
- Marketing start
- 2022-09-15
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0536-1373-37 | 00536137337 | 1 BOTTLE in 1 PACKAGE (0536-1373-37) > 60 SPRAY, METERED in 1 BOTTLE | 1 bottle | 2022-09-15 | 0000-00-00 | No | No | Current |
| 0536-1373-38 | 00536137338 | 1 BOTTLE in 1 PACKAGE (0536-1373-38) > 120 SPRAY, METERED in 1 BOTTLE | 1 bottle | 2022-09-15 | 0000-00-00 | No | No | Current |