ADVAIR
- Product NDC
- 70518-0514
- 11-digit product format
- 705180514
- Labeler code
- 70518
- Product ID
- 70518-0514_beb04da3-1a75-63eb-e053-2a95a90ab1e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluticasone propionate and salmeterol
- Dosage form
- POWDER
- Route
- RESPIRATORY (INHALATION)
- Labeler
- REMEDYREPACK INC.
- Application
- NDA021077
- Marketing category
- NDA
- Marketing start
- 2017-05-10
- Marketing end
- 0000-00-00
- Substance
- SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE
- Active strength
- 50 ug/1; ug/1
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-0514-0 | 70518051400 | 1 INHALER in 1 CARTON (70518-0514-0) > 60 POWDER in 1 INHALER | 1 inhaler | 2017-05-10 | 0000-00-00 | No | No | Current |