ADVAIR
- Product NDC
- 70518-0508
- 11-digit product format
- 705180508
- Labeler code
- 70518
- Product ID
- 70518-0508_8591003c-c2f7-df65-e053-2a91aa0a42fb
- 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
- 2017-05-09
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record