leader allergy relief nasal
- Product NDC
- 70000-0110
- 11-digit product format
- 700000110
- Labeler code
- 70000
- Product ID
- 70000-0110_a4440b09-5cc0-4394-b00c-75987cc911bf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fluticasone propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Cardinal Health 110, LLC. dba Leader
- Application
- ANDA207957
- Marketing category
- ANDA
- Marketing start
- 2016-05-27
- 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 |
|---|
| 70000-0110 | LEADER ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [CARDINAL HEALTH 110, LLC. DBA LEADER] | 6 | Legacy NDC | 20221115_90dfc92b-8db7-4d8e-8190-190f5a1dcc0e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70000-0110-1 | 70000011001 | 1 BOTTLE in 1 CARTON (70000-0110-1) > 120 SPRAY, METERED in 1 BOTTLE | 1 bottle | 2016-06-22 | 0000-00-00 | No | No | Current |